Canonical Allele Identifier: CA403668642

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117272T>A (hg19) ; chr19:g.7117261T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3944A>T MANE Select	ENSP00000303830.4:p.Glu1315Val
ENST00000302850.9:c.3944A>T	ENSP00000303830.4:p.Glu1315Val
ENST00000341500.9:c.3908A>T	ENSP00000342838.4:p.Glu1303Val
NM_000208.2:c.3944A>T	NP_000199.2:p.Glu1315Val
NM_000208.3:c.3944A>T	NP_000199.2:p.Glu1315Val
NM_001079817.1:c.3908A>T	NP_001073285.1:p.Glu1303Val
NM_001079817.2:c.3908A>T	NP_001073285.1:p.Glu1303Val
XM_011527988.1:c.4019A>T	XP_011526290.1:p.Glu1340Val
XM_011527989.1:c.3983A>T	XP_011526291.1:p.Glu1328Val
XM_011527988.2:c.3941A>T	XP_011526290.2:p.Glu1314Val
XM_011527989.3:c.3905A>T	XP_011526291.2:p.Glu1302Val
NM_000208.4:c.3944A>T MANE Select	NP_000199.2:p.Glu1315Val
NM_001079817.3:c.3908A>T	NP_001073285.1:p.Glu1303Val