Canonical Allele Identifier: CA124211
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 14679
ClinVar RCV Id: RCV000015793
dbSNP Id: rs121913135

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7125437C>A , CM000681.2:g.7125437C>A GRCh38
NC_000019.9:g.7125448C>A , CM000681.1:g.7125448C>A GRCh37
NC_000019.8:g.7076448C>A NCBI36
NG_008852.2:g.173564G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.3104G>T MANE Select ENSP00000303830.4:p.Gly1035Val
ENST00000302850.9:c.3104G>T ENSP00000303830.4:p.Gly1035Val
ENST00000341500.9:c.3068G>T ENSP00000342838.4:p.Gly1023Val
NM_000208.2:c.3104G>T NP_000199.2:p.Gly1035Val
NM_000208.3:c.3104G>T NP_000199.2:p.Gly1035Val
NM_001079817.1:c.3068G>T NP_001073285.1:p.Gly1023Val
NM_001079817.2:c.3068G>T NP_001073285.1:p.Gly1023Val
XM_011527988.1:c.3179G>T XP_011526290.1:p.Gly1060Val
XM_011527989.1:c.3143G>T XP_011526291.1:p.Gly1048Val
XM_011527988.2:c.3101G>T XP_011526290.2:p.Gly1034Val
XM_011527989.3:c.3065G>T XP_011526291.2:p.Gly1022Val
NM_000208.4:c.3104G>T MANE Select NP_000199.2:p.Gly1035Val
NM_001079817.3:c.3068G>T NP_001073285.1:p.Gly1023Val