Canonical Allele Identifier: CA13341817
Gene: ANK3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1002442

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.60043304T>G , CM000672.2:g.60043304T>G GRCh38
NC_000010.10:g.61803062T>G , CM000672.1:g.61803062T>G GRCh37
NC_000010.9:g.61473068T>G NCBI36
NG_029917.1:g.695223A>C

Transcript Alleles

HGVS Amino-acid change
NM_001149.3:c.2938-545A>C VV NP_001140.2:p.=
NM_001204403.1:c.5518-545A>C VV NP_001191332.1:p.=
NM_001204404.1:c.5539-545A>C VV NP_001191333.1:p.=
NM_020987.3:c.13066-545A>C VV NP_066267.2:p.=
XM_005269715.2:c.5590-545A>C XP_005269772.1:p.=
XM_005269716.2:c.5536-545A>C XP_005269773.1:p.=
XM_006717791.2:c.8494-548A>C XP_006717854.1:p.=
XM_006717793.2:c.8434-545A>C XP_006717856.1:p.=
XM_006717795.2:c.8263-548A>C XP_006717858.1:p.=
XM_006717796.2:c.8212-548A>C XP_006717859.1:p.=
XM_006717802.2:c.5629-545A>C XP_006717865.1:p.=
XM_011539700.1:c.8482-545A>C XP_011538002.1:p.=
XM_011539701.1:c.8476-545A>C XP_011538003.1:p.=
XM_011539702.1:c.8437-545A>C XP_011538004.1:p.=
XM_011539703.1:c.8416-545A>C XP_011538005.1:p.=
XM_011539704.1:c.8395-545A>C XP_011538006.1:p.=
XM_011539705.1:c.8395-545A>C XP_011538007.1:p.=
XM_011539706.1:c.8383-545A>C XP_011538008.1:p.=
XM_011539707.1:c.8263-545A>C XP_011538009.1:p.=
XM_011539708.1:c.8212-545A>C XP_011538010.1:p.=
XM_011539709.1:c.7903-545A>C XP_011538011.1:p.=
XM_011539710.1:c.5911-545A>C XP_011538012.1:p.=
XM_011539711.1:c.5884-545A>C XP_011538013.1:p.=
XM_011539712.1:c.5875-545A>C XP_011538014.1:p.=
XM_011539713.1:c.5848-545A>C XP_011538015.1:p.=
XM_011539714.1:c.5842-545A>C XP_011538016.1:p.=
XM_011539715.1:c.5830-545A>C XP_011538017.1:p.=
XM_011539716.1:c.5704-545A>C XP_011538018.1:p.=
XM_011539717.1:c.5563-545A>C XP_011538019.1:p.=
XM_011539718.1:c.5446-545A>C XP_011538020.1:p.=
NM_001320874.1:c.5536-545A>C VV NP_001307803.1:p.=
NM_020987.4:c.13066-545A>C VV NP_066267.2:p.=
XM_005269715.3:c.5590-545A>C XP_005269772.1:p.=
XM_006717796.3:c.8212-548A>C XP_006717859.1:p.=
XM_006717802.3:c.5629-545A>C XP_006717865.1:p.=
XM_011539708.2:c.8212-545A>C XP_011538010.1:p.=
XM_011539709.2:c.7903-545A>C XP_011538011.1:p.=
XM_017016110.1:c.13447-545A>C XP_016871599.1:p.=
XM_017016111.1:c.13435-545A>C XP_016871600.1:p.=
XM_017016112.1:c.13432-545A>C XP_016871601.1:p.=
XM_017016113.1:c.13420-545A>C XP_016871602.1:p.=
XM_017016114.1:c.13396-545A>C XP_016871603.1:p.=
XM_017016115.1:c.13369-545A>C XP_016871604.1:p.=
XM_017016116.1:c.13138-545A>C XP_016871605.1:p.=
XM_017016117.1:c.13138-548A>C XP_016871606.1:p.=
XM_017016118.1:c.12106-545A>C XP_016871607.1:p.=
XM_017016119.1:c.11797-545A>C XP_016871608.1:p.=
XM_017016120.1:c.11797-548A>C XP_016871609.1:p.=
XM_017016121.1:c.11770-545A>C XP_016871610.1:p.=
XM_017016122.1:c.8119-545A>C XP_016871611.1:p.=
XM_017016123.1:c.7903-548A>C XP_016871612.1:p.=
XM_017016124.1:c.7876-545A>C XP_016871613.1:p.=
XM_017016125.1:c.7876-548A>C XP_016871614.1:p.=
XM_017016126.1:c.7771-545A>C XP_016871615.1:p.=
XM_017016127.1:c.7744-545A>C XP_016871616.1:p.=
XM_017016128.1:c.5602-545A>C XP_016871617.1:p.=
XM_017016129.1:c.5602-548A>C XP_016871618.1:p.=
XM_017016130.1:c.5536-548A>C XP_016871619.1:p.=
XM_017016131.1:c.5521-545A>C XP_016871620.1:p.=
XM_017016132.1:c.5500-545A>C XP_016871621.1:p.=
XM_017016134.1:c.5470-545A>C XP_016871623.1:p.=
XM_017016136.1:c.5320-545A>C XP_016871625.1:p.=
XM_017016137.1:c.5293-545A>C XP_016871626.1:p.=
XM_017016138.1:c.5293-548A>C XP_016871627.1:p.=
XM_017016141.1:c.5188-545A>C XP_016871630.1:p.=
XM_024447953.1:c.13420-545A>C XP_024303721.1:p.=
XM_024447954.1:c.13393-545A>C XP_024303722.1:p.=
XM_024447955.1:c.13384-545A>C XP_024303723.1:p.=
XM_024447956.1:c.13381-545A>C XP_024303724.1:p.=
XM_024447957.1:c.13348-545A>C XP_024303725.1:p.=
XM_024447958.1:c.13330-545A>C XP_024303726.1:p.=
XM_024447959.1:c.13330-545A>C XP_024303727.1:p.=
XM_024447960.1:c.13318-545A>C XP_024303728.1:p.=
XM_024447961.1:c.13315-545A>C XP_024303729.1:p.=
XM_024447962.1:c.12346-545A>C XP_024303730.1:p.=
XM_024447963.1:c.8479-548A>C XP_024303731.1:p.=
XM_024447964.1:c.5833-545A>C XP_024303732.1:p.=
XM_024447965.1:c.5593-545A>C XP_024303733.1:p.=
NM_020987.5:c.13066-545A>C VV MANE Preferred NP_066267.2:p.=
ENST00000280772.6:c.13066-545A>C ENSP00000280772.1:p.=
ENST00000355288.6:c.2938-545A>C ENSP00000347436.2:p.=
ENST00000373820.5:n.1312-545A>C ENSP00000362926.1:p.=
ENST00000373827.6:c.5518-545A>C ENSP00000362933.2:p.=
ENST00000480699.5:n.275-545A>C
ENST00000489505.2:n.1500A>C
ENST00000502769.5:n.433-545A>C ENSP00000423057.1:p.=
ENST00000503366.5:c.5539-545A>C ENSP00000425236.1:p.=
ENST00000610321.4:n.4862-545A>C
ENST00000612776.4:n.471-548A>C
ENST00000616444.4:n.2852-545A>C
ENST00000617800.4:n.458-545A>C
ENST00000618374.4:c.*501-545A>C ENSP00000479018.1:p.=