Canonical Allele Identifier: CA403671192

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125400T>C (hg19) ; chr19:g.7125389T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125389T>C , CM000681.2:g.7125389T>C	GRCh38
NC_000019.9:g.7125400T>C , CM000681.1:g.7125400T>C	GRCh37
NC_000019.8:g.7076400T>C	NCBI36
NG_008852.2:g.173612A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3152A>G MANE Select	ENSP00000303830.4:p.Glu1051Gly
ENST00000302850.9:c.3152A>G	ENSP00000303830.4:p.Glu1051Gly
ENST00000341500.9:c.3116A>G	ENSP00000342838.4:p.Glu1039Gly
NM_000208.2:c.3152A>G	NP_000199.2:p.Glu1051Gly
NM_000208.3:c.3152A>G	NP_000199.2:p.Glu1051Gly
NM_001079817.1:c.3116A>G	NP_001073285.1:p.Glu1039Gly
NM_001079817.2:c.3116A>G	NP_001073285.1:p.Glu1039Gly
XM_011527988.1:c.3227A>G	XP_011526290.1:p.Glu1076Gly
XM_011527989.1:c.3191A>G	XP_011526291.1:p.Glu1064Gly
XM_011527988.2:c.3149A>G	XP_011526290.2:p.Glu1050Gly
XM_011527989.3:c.3113A>G	XP_011526291.2:p.Glu1038Gly
NM_000208.4:c.3152A>G MANE Select	NP_000199.2:p.Glu1051Gly
NM_001079817.3:c.3116A>G	NP_001073285.1:p.Glu1039Gly