Canonical Allele Identifier: CA403671960

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7132198T>A (hg19) ; chr19:g.7132187T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132187T>A , CM000681.2:g.7132187T>A	GRCh38
NC_000019.9:g.7132198T>A , CM000681.1:g.7132198T>A	GRCh37
NC_000019.8:g.7083198T>A	NCBI36
NG_008852.2:g.166814A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2813A>T MANE Select	ENSP00000303830.4:p.Glu938Val
ENST00000302850.9:c.2813A>T	ENSP00000303830.4:p.Glu938Val
ENST00000341500.9:c.2777A>T	ENSP00000342838.4:p.Glu926Val
NM_000208.2:c.2813A>T	NP_000199.2:p.Glu938Val
NM_000208.3:c.2813A>T	NP_000199.2:p.Glu938Val
NM_001079817.1:c.2777A>T	NP_001073285.1:p.Glu926Val
NM_001079817.2:c.2777A>T	NP_001073285.1:p.Glu926Val
XM_011527988.1:c.2891A>T	XP_011526290.1:p.Glu964Val
XM_011527989.1:c.2855A>T	XP_011526291.1:p.Glu952Val
XM_011527988.2:c.2813A>T	XP_011526290.2:p.Glu938Val
XM_011527989.3:c.2777A>T	XP_011526291.2:p.Glu926Val
NM_000208.4:c.2813A>T MANE Select	NP_000199.2:p.Glu938Val
NM_001079817.3:c.2777A>T	NP_001073285.1:p.Glu926Val