Canonical Allele Identifier: CA403668728

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117308A>T (hg19) ; chr19:g.7117297A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117297A>T , CM000681.2:g.7117297A>T	GRCh38
NC_000019.9:g.7117308A>T , CM000681.1:g.7117308A>T	GRCh37
NC_000019.8:g.7068308A>T	NCBI36
NG_008852.2:g.181704T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3908T>A MANE Select	ENSP00000303830.4:p.Phe1303Tyr
ENST00000302850.9:c.3908T>A	ENSP00000303830.4:p.Phe1303Tyr
ENST00000341500.9:c.3872T>A	ENSP00000342838.4:p.Phe1291Tyr
NM_000208.2:c.3908T>A	NP_000199.2:p.Phe1303Tyr
NM_000208.3:c.3908T>A	NP_000199.2:p.Phe1303Tyr
NM_001079817.1:c.3872T>A	NP_001073285.1:p.Phe1291Tyr
NM_001079817.2:c.3872T>A	NP_001073285.1:p.Phe1291Tyr
XM_011527988.1:c.3983T>A	XP_011526290.1:p.Phe1328Tyr
XM_011527989.1:c.3947T>A	XP_011526291.1:p.Phe1316Tyr
XM_011527988.2:c.3905T>A	XP_011526290.2:p.Phe1302Tyr
XM_011527989.3:c.3869T>A	XP_011526291.2:p.Phe1290Tyr
NM_000208.4:c.3908T>A MANE Select	NP_000199.2:p.Phe1303Tyr
NM_001079817.3:c.3872T>A	NP_001073285.1:p.Phe1291Tyr