Canonical Allele Identifier: CA124215
Gene: INSR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 14681
ClinVar RCV Id: RCV000015795
dbSNP Id: rs267607184

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7172381C>T , CM000681.2:g.7172381C>T GRCh38
NC_000019.9:g.7172392C>T , CM000681.1:g.7172392C>T GRCh37
NC_000019.8:g.7123392C>T NCBI36
NG_008852.2:g.126620G>A

Transcript Alleles

HGVS Amino-acid change
NM_000208.2:c.1177G>A VV NP_000199.2:p.Gly393Arg
NM_000208.3:c.1177G>A VV NP_000199.2:p.Gly393Arg
NM_001079817.1:c.1177G>A VV NP_001073285.1:p.Gly393Arg
NM_001079817.2:c.1177G>A VV NP_001073285.1:p.Gly393Arg
XM_011527988.1:c.1255G>A XP_011526290.1:p.Gly419Arg
XM_011527989.1:c.1255G>A XP_011526291.1:p.Gly419Arg
XM_011527988.2:c.1177G>A XP_011526290.2:p.Gly393Arg
XM_011527989.3:c.1177G>A XP_011526291.2:p.Gly393Arg
NM_000208.4:c.1177G>A VV MANE Preferred NP_000199.2:p.Gly393Arg
ENST00000302850.9:c.1177G>A ENSP00000303830.4:p.Gly393Arg
ENST00000341500.9:c.1177G>A ENSP00000342838.4:p.Gly393Arg
ENST00000598216.1:n.1152G>A