Canonical Allele Identifier: CA403671902

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7132172A>C (hg19) ; chr19:g.7132161A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132161A>C , CM000681.2:g.7132161A>C	GRCh38
NC_000019.9:g.7132172A>C , CM000681.1:g.7132172A>C	GRCh37
NC_000019.8:g.7083172A>C	NCBI36
NG_008852.2:g.166840T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2839T>G MANE Select	ENSP00000303830.4:p.Tyr947Asp
ENST00000302850.9:c.2839T>G	ENSP00000303830.4:p.Tyr947Asp
ENST00000341500.9:c.2803T>G	ENSP00000342838.4:p.Tyr935Asp
NM_000208.2:c.2839T>G	NP_000199.2:p.Tyr947Asp
NM_000208.3:c.2839T>G	NP_000199.2:p.Tyr947Asp
NM_001079817.1:c.2803T>G	NP_001073285.1:p.Tyr935Asp
NM_001079817.2:c.2803T>G	NP_001073285.1:p.Tyr935Asp
XM_011527988.1:c.2917T>G	XP_011526290.1:p.Tyr973Asp
XM_011527989.1:c.2881T>G	XP_011526291.1:p.Tyr961Asp
XM_011527988.2:c.2839T>G	XP_011526290.2:p.Tyr947Asp
XM_011527989.3:c.2803T>G	XP_011526291.2:p.Tyr935Asp
NM_000208.4:c.2839T>G MANE Select	NP_000199.2:p.Tyr947Asp
NM_001079817.3:c.2803T>G	NP_001073285.1:p.Tyr935Asp