Canonical Allele Identifier: CA403668641

Gene: INSR

Linked Data

• dbSNP Id: rs1232668568
• gnomAD v2: 19-7117272-T-G
• gnomAD v4: 19-7117261-T-G
• MyVariant Identifiers: chr19:g.7117272T>G (hg19) ; chr19:g.7117261T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117261T>G , CM000681.2:g.7117261T>G	GRCh38
NC_000019.9:g.7117272T>G , CM000681.1:g.7117272T>G	GRCh37
NC_000019.8:g.7068272T>G	NCBI36
NG_008852.2:g.181740A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3944A>C MANE Select	ENSP00000303830.4:p.Glu1315Ala
ENST00000302850.9:c.3944A>C	ENSP00000303830.4:p.Glu1315Ala
ENST00000341500.9:c.3908A>C	ENSP00000342838.4:p.Glu1303Ala
NM_000208.2:c.3944A>C	NP_000199.2:p.Glu1315Ala
NM_000208.3:c.3944A>C	NP_000199.2:p.Glu1315Ala
NM_001079817.1:c.3908A>C	NP_001073285.1:p.Glu1303Ala
NM_001079817.2:c.3908A>C	NP_001073285.1:p.Glu1303Ala
XM_011527988.1:c.4019A>C	XP_011526290.1:p.Glu1340Ala
XM_011527989.1:c.3983A>C	XP_011526291.1:p.Glu1328Ala
XM_011527988.2:c.3941A>C	XP_011526290.2:p.Glu1314Ala
XM_011527989.3:c.3905A>C	XP_011526291.2:p.Glu1302Ala
NM_000208.4:c.3944A>C MANE Select	NP_000199.2:p.Glu1315Ala
NM_001079817.3:c.3908A>C	NP_001073285.1:p.Glu1303Ala