Canonical Allele Identifier: CA622684165
Gene: KATNB1 HGNC NCBI

Linked Data

dbSNP Id: rs1555583127
MyVariant Identifiers: chr16:g.57785549T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.57751637T>G , CM000678.2:g.57751637T>G GRCh38
NC_000016.9:g.57785549T>G , CM000678.1:g.57785549T>G GRCh37
NC_000016.8:g.56343050T>G NCBI36
NG_046947.1:g.20918T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000379661.8:c.433-4T>G MANE Select ENSP00000368982.3:n.433-4T>G
ENST00000379661.7:c.433-4T>G ENSP00000368982.3:n.433-4T>G
ENST00000562592.5:c.433-4T>G ENSP00000455350.1:n.433-4T>G
ENST00000563127.1:n.485-4T>G
ENST00000566611.5:n.952-4T>G
ENST00000566726.5:c.445-4T>G ENSP00000455270.1:n.445-4T>G
ENST00000569627.1:c.332-4T>G ENSP00000457046.1:n.332-4T>G
NM_005886.2:c.433-4T>G NP_005877.2:n.433-4T>G
XM_005255772.3:c.433-4T>G XP_005255829.1:n.433-4T>G
XM_006721121.2:c.433-4T>G XP_006721184.1:n.433-4T>G
XM_006721122.2:c.433-4T>G XP_006721185.1:n.433-4T>G
XM_006721123.2:c.433-4T>G XP_006721186.1:n.433-4T>G
XM_011522810.1:c.433-4T>G XP_011521112.1:n.433-4T>G
XM_005255772.5:c.433-4T>G XP_005255829.1:n.433-4T>G
XM_006721121.4:c.433-4T>G XP_006721184.1:n.433-4T>G
XM_006721123.4:c.433-4T>G XP_006721186.1:n.433-4T>G
XM_011522810.2:c.433-4T>G XP_011521112.1:n.433-4T>G
XM_017022860.2:c.433-4T>G XP_016878349.1:n.433-4T>G
XM_017022861.1:c.433-4T>G XP_016878350.1:n.433-4T>G
XM_017022862.1:c.433-4T>G XP_016878351.1:n.433-4T>G
XM_017022863.1:c.433-4T>G XP_016878352.1:n.433-4T>G
XM_017022864.1:c.433-4T>G XP_016878353.1:n.433-4T>G
NM_005886.3:c.433-4T>G MANE Select NP_005877.2:n.433-4T>G