Canonical Allele Identifier: CA403668433

Gene: INSR

Linked Data

• COSMIC: COSM48428
• MyVariant Identifiers: chr19:g.7117179C>T (hg19) ; chr19:g.7117168C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117168C>T , CM000681.2:g.7117168C>T	GRCh38
NC_000019.9:g.7117179C>T , CM000681.1:g.7117179C>T	GRCh37
NC_000019.8:g.7068179C>T	NCBI36
NG_008852.2:g.181833G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4037G>A MANE Select	ENSP00000303830.4:p.Gly1346Glu
ENST00000302850.9:c.4037G>A	ENSP00000303830.4:p.Gly1346Glu
ENST00000341500.9:c.4001G>A	ENSP00000342838.4:p.Gly1334Glu
NM_000208.2:c.4037G>A	NP_000199.2:p.Gly1346Glu
NM_000208.3:c.4037G>A	NP_000199.2:p.Gly1346Glu
NM_001079817.1:c.4001G>A	NP_001073285.1:p.Gly1334Glu
NM_001079817.2:c.4001G>A	NP_001073285.1:p.Gly1334Glu
XM_011527988.1:c.4112G>A	XP_011526290.1:p.Gly1371Glu
XM_011527989.1:c.4076G>A	XP_011526291.1:p.Gly1359Glu
XM_011527988.2:c.4034G>A	XP_011526290.2:p.Gly1345Glu
XM_011527989.3:c.3998G>A	XP_011526291.2:p.Gly1333Glu
NM_000208.4:c.4037G>A MANE Select	NP_000199.2:p.Gly1346Glu
NM_001079817.3:c.4001G>A	NP_001073285.1:p.Gly1334Glu