Canonical Allele Identifier: CA403671312

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125452A>T (hg19) ; chr19:g.7125441A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125441A>T , CM000681.2:g.7125441A>T	GRCh38
NC_000019.9:g.7125452A>T , CM000681.1:g.7125452A>T	GRCh37
NC_000019.8:g.7076452A>T	NCBI36
NG_008852.2:g.173560T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3100T>A MANE Select	ENSP00000303830.4:p.Phe1034Ile
ENST00000302850.9:c.3100T>A	ENSP00000303830.4:p.Phe1034Ile
ENST00000341500.9:c.3064T>A	ENSP00000342838.4:p.Phe1022Ile
NM_000208.2:c.3100T>A	NP_000199.2:p.Phe1034Ile
NM_000208.3:c.3100T>A	NP_000199.2:p.Phe1034Ile
NM_001079817.1:c.3064T>A	NP_001073285.1:p.Phe1022Ile
NM_001079817.2:c.3064T>A	NP_001073285.1:p.Phe1022Ile
XM_011527988.1:c.3175T>A	XP_011526290.1:p.Phe1059Ile
XM_011527989.1:c.3139T>A	XP_011526291.1:p.Phe1047Ile
XM_011527988.2:c.3097T>A	XP_011526290.2:p.Phe1033Ile
XM_011527989.3:c.3061T>A	XP_011526291.2:p.Phe1021Ile
NM_000208.4:c.3100T>A MANE Select	NP_000199.2:p.Phe1034Ile
NM_001079817.3:c.3064T>A	NP_001073285.1:p.Phe1022Ile