Canonical Allele Identifier: CA124264
Gene: INSR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 14708
dbSNP Id: rs121913156

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7120677C>T , CM000681.2:g.7120677C>T GRCh38
NC_000019.9:g.7120688C>T , CM000681.1:g.7120688C>T GRCh37
NC_000019.8:g.7071688C>T NCBI36
NG_008852.2:g.178324G>A

Transcript Alleles

HGVS Amino-acid change
NM_000208.2:c.3602G>A VV
NM_000208.3:c.3602G>A VV NP_000199.2:p.Arg1201Gln
NM_001079817.1:c.3566G>A VV
NM_001079817.2:c.3566G>A VV NP_001073285.1:p.Arg1189Gln
XM_011527988.1:c.3677G>A XP_011526290.1:p.Arg1226Gln
XM_011527989.1:c.3641G>A XP_011526291.1:p.Arg1214Gln
XM_011527988.2:c.3599G>A XP_011526290.2:p.Arg1200Gln
XM_011527989.3:c.3563G>A XP_011526291.2:p.Arg1188Gln
NM_000208.4:c.3602G>A VV MANE Preferred
ENST00000302850.9:c.3602G>A ENSP00000303830.4:p.Arg1201Gln
ENST00000341500.9:c.3566G>A ENSP00000342838.4:p.Arg1189Gln
ENST00000601099.1:n.513G>A