Canonical Allele Identifier: CA403668744

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117316C>A (hg19) ; chr19:g.7117305C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117305C>A , CM000681.2:g.7117305C>A	GRCh38
NC_000019.9:g.7117316C>A , CM000681.1:g.7117316C>A	GRCh37
NC_000019.8:g.7068316C>A	NCBI36
NG_008852.2:g.181696G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3900G>T MANE Select	ENSP00000303830.4:p.Glu1300Asp
ENST00000302850.9:c.3900G>T	ENSP00000303830.4:p.Glu1300Asp
ENST00000341500.9:c.3864G>T	ENSP00000342838.4:p.Glu1288Asp
NM_000208.2:c.3900G>T	NP_000199.2:p.Glu1300Asp
NM_000208.3:c.3900G>T	NP_000199.2:p.Glu1300Asp
NM_001079817.1:c.3864G>T	NP_001073285.1:p.Glu1288Asp
NM_001079817.2:c.3864G>T	NP_001073285.1:p.Glu1288Asp
XM_011527988.1:c.3975G>T	XP_011526290.1:p.Glu1325Asp
XM_011527989.1:c.3939G>T	XP_011526291.1:p.Glu1313Asp
XM_011527988.2:c.3897G>T	XP_011526290.2:p.Glu1299Asp
XM_011527989.3:c.3861G>T	XP_011526291.2:p.Glu1287Asp
NM_000208.4:c.3900G>T MANE Select	NP_000199.2:p.Glu1300Asp
NM_001079817.3:c.3864G>T	NP_001073285.1:p.Glu1288Asp