Canonical Allele Identifier: CA403671719

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7128890C>T (hg19) ; chr19:g.7128879C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128879C>T , CM000681.2:g.7128879C>T	GRCh38
NC_000019.9:g.7128890C>T , CM000681.1:g.7128890C>T	GRCh37
NC_000019.8:g.7079890C>T	NCBI36
NG_008852.2:g.170122G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2918G>A MANE Select	ENSP00000303830.4:p.Gly973Glu
ENST00000302850.9:c.2918G>A	ENSP00000303830.4:p.Gly973Glu
ENST00000341500.9:c.2882G>A	ENSP00000342838.4:p.Gly961Glu
NM_000208.2:c.2918G>A	NP_000199.2:p.Gly973Glu
NM_000208.3:c.2918G>A	NP_000199.2:p.Gly973Glu
NM_001079817.1:c.2882G>A	NP_001073285.1:p.Gly961Glu
NM_001079817.2:c.2882G>A	NP_001073285.1:p.Gly961Glu
XM_011527988.1:c.2993G>A	XP_011526290.1:p.Gly998Glu
XM_011527989.1:c.2957G>A	XP_011526291.1:p.Gly986Glu
XM_011527988.2:c.2915G>A	XP_011526290.2:p.Gly972Glu
XM_011527989.3:c.2879G>A	XP_011526291.2:p.Gly960Glu
NM_000208.4:c.2918G>A MANE Select	NP_000199.2:p.Gly973Glu
NM_001079817.3:c.2882G>A	NP_001073285.1:p.Gly961Glu