Canonical Allele Identifier: CA505217397

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7128916A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128905A>G , CM000681.2:g.7128905A>G	GRCh38
NC_000019.9:g.7128916A>G , CM000681.1:g.7128916A>G	GRCh37
NC_000019.8:g.7079916A>G	NCBI36
NG_008852.2:g.170096T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2892T>C MANE Select	ENSP00000303830.4:p.Phe964=
ENST00000302850.9:c.2892T>C	ENSP00000303830.4:p.Phe964=
ENST00000341500.9:c.2856T>C	ENSP00000342838.4:p.Phe952=
NM_000208.2:c.2892T>C	NP_000199.2:p.Phe964=
NM_000208.3:c.2892T>C	NP_000199.2:p.Phe964=
NM_001079817.1:c.2856T>C	NP_001073285.1:p.Phe952=
NM_001079817.2:c.2856T>C	NP_001073285.1:p.Phe952=
XM_011527988.1:c.2967T>C	XP_011526290.1:p.Phe989=
XM_011527989.1:c.2931T>C	XP_011526291.1:p.Phe977=
XM_011527988.2:c.2889T>C	XP_011526290.2:p.Phe963=
XM_011527989.3:c.2853T>C	XP_011526291.2:p.Phe951=
NM_000208.4:c.2892T>C MANE Select	NP_000199.2:p.Phe964=
NM_001079817.3:c.2856T>C	NP_001073285.1:p.Phe952=