Canonical Allele Identifier: CA403671803

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7128929C>A (hg19) ; chr19:g.7128918C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128918C>A , CM000681.2:g.7128918C>A	GRCh38
NC_000019.9:g.7128929C>A , CM000681.1:g.7128929C>A	GRCh37
NC_000019.8:g.7079929C>A	NCBI36
NG_008852.2:g.170083G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2879G>T MANE Select	ENSP00000303830.4:p.Gly960Val
ENST00000302850.9:c.2879G>T	ENSP00000303830.4:p.Gly960Val
ENST00000341500.9:c.2843G>T	ENSP00000342838.4:p.Gly948Val
NM_000208.2:c.2879G>T	NP_000199.2:p.Gly960Val
NM_000208.3:c.2879G>T	NP_000199.2:p.Gly960Val
NM_001079817.1:c.2843G>T	NP_001073285.1:p.Gly948Val
NM_001079817.2:c.2843G>T	NP_001073285.1:p.Gly948Val
XM_011527988.1:c.2954G>T	XP_011526290.1:p.Gly985Val
XM_011527989.1:c.2918G>T	XP_011526291.1:p.Gly973Val
XM_011527988.2:c.2876G>T	XP_011526290.2:p.Gly959Val
XM_011527989.3:c.2840G>T	XP_011526291.2:p.Gly947Val
NM_000208.4:c.2879G>T MANE Select	NP_000199.2:p.Gly960Val
NM_001079817.3:c.2843G>T	NP_001073285.1:p.Gly948Val