Canonical Allele Identifier: CA605120075
Gene: AMHR2 HGNC NCBI

Linked Data

dbSNP Id: rs1278175660

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53430107del , CM000674.2:g.53430107del GRCh38
NC_000012.11:g.53823891del , CM000674.1:g.53823891del GRCh37
NC_000012.10:g.52110158del NCBI36
NG_015981.1:g.11253del

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1289-39del MANE Select ENSP00000257863.3:n.1289-39del
ENST00000257863.8:c.1289-39del ENSP00000257863.3:n.1289-39del
ENST00000379791.7:c.1140+482del ENSP00000369117.3:n.1140+482del
ENST00000550311.5:c.1289-43del ENSP00000446661.1:n.1289-43del
ENST00000550839.1:c.380-39del ENSP00000455338.1:n.380-39del
ENST00000552233.5:n.1005del
NM_001164690.1:c.1289-43del NP_001158162.1:n.1289-43del
NM_001164691.1:c.1140+482del NP_001158163.1:n.1140+482del
NM_020547.2:c.1289-39del NP_065434.1:n.1289-39del
XM_011538173.1:c.1349-39del XP_011536475.1:n.1349-39del
XM_011538174.1:c.1346-39del XP_011536476.1:n.1346-39del
XM_011538175.1:c.1331-39del XP_011536477.1:n.1331-39del
XM_011538176.1:c.1292-39del XP_011536478.1:n.1292-39del
XM_011538177.1:c.1271-39del XP_011536479.1:n.1271-39del
XM_011538178.1:c.1130-39del XP_011536480.1:n.1130-39del
XM_011538179.1:c.1200+482del XP_011536481.1:n.1200+482del
XM_011538180.1:c.1016-39del XP_011536482.1:n.1016-39del
XM_011538181.1:c.1013-39del XP_011536483.1:n.1013-39del
XM_011538182.1:c.938-39del XP_011536484.1:n.938-39del
XM_011538183.1:c.1201-39del XP_011536485.1:n.1201-39del
XM_011538184.1:c.1220+462del XP_011536486.1:n.1220+462del
XM_011538185.1:c.856-1070del XP_011536487.1:n.856-1070del
XM_011538186.1:c.464-39del XP_011536488.1:n.464-39del
NM_001164690.2:c.1289-43del NP_001158162.1:n.1289-43del
NM_001164691.2:c.1140+482del NP_001158163.1:n.1140+482del
NM_020547.3:c.1289-39del MANE Select NP_065434.1:n.1289-39del
XM_011538183.2:c.1201-39del XP_011536485.1:n.1201-39del
XM_011538184.2:c.1220+462del XP_011536486.1:n.1220+462del
XM_011538186.3:c.464-39del XP_011536488.1:n.464-39del
XM_017019179.2:c.1348+129del XP_016874668.1:n.1348+129del
XM_024448938.1:c.1143+482del XP_024304706.1:n.1143+482del
XR_002957309.1:n.1257-39del
XR_002957310.1:n.1109-39del
XR_002957311.1:n.1256+129del
XR_002957312.1:n.1108+482del