Canonical Allele Identifier: CA403671687

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7128876A>T (hg19) ; chr19:g.7128865A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128865A>T , CM000681.2:g.7128865A>T	GRCh38
NC_000019.9:g.7128876A>T , CM000681.1:g.7128876A>T	GRCh37
NC_000019.8:g.7079876A>T	NCBI36
NG_008852.2:g.170136T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2932T>A MANE Select	ENSP00000303830.4:p.Phe978Ile
ENST00000302850.9:c.2932T>A	ENSP00000303830.4:p.Phe978Ile
ENST00000341500.9:c.2896T>A	ENSP00000342838.4:p.Phe966Ile
NM_000208.2:c.2932T>A	NP_000199.2:p.Phe978Ile
NM_000208.3:c.2932T>A	NP_000199.2:p.Phe978Ile
NM_001079817.1:c.2896T>A	NP_001073285.1:p.Phe966Ile
NM_001079817.2:c.2896T>A	NP_001073285.1:p.Phe966Ile
XM_011527988.1:c.3007T>A	XP_011526290.1:p.Phe1003Ile
XM_011527989.1:c.2971T>A	XP_011526291.1:p.Phe991Ile
XM_011527988.2:c.2929T>A	XP_011526290.2:p.Phe977Ile
XM_011527989.3:c.2893T>A	XP_011526291.2:p.Phe965Ile
NM_000208.4:c.2932T>A MANE Select	NP_000199.2:p.Phe978Ile
NM_001079817.3:c.2896T>A	NP_001073285.1:p.Phe966Ile