Canonical Allele Identifier: CA505400006

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117130T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117119T>G , CM000681.2:g.7117119T>G	GRCh38
NC_000019.9:g.7117130T>G , CM000681.1:g.7117130T>G	GRCh37
NC_000019.8:g.7068130T>G	NCBI36
NG_008852.2:g.181882A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4086A>C MANE Select	ENSP00000303830.4:p.Thr1362=
ENST00000302850.9:c.4086A>C	ENSP00000303830.4:p.Thr1362=
ENST00000341500.9:c.4050A>C	ENSP00000342838.4:p.Thr1350=
NM_000208.2:c.4086A>C	NP_000199.2:p.Thr1362=
NM_000208.3:c.4086A>C	NP_000199.2:p.Thr1362=
NM_001079817.1:c.4050A>C	NP_001073285.1:p.Thr1350=
NM_001079817.2:c.4050A>C	NP_001073285.1:p.Thr1350=
XM_011527988.1:c.4161A>C	XP_011526290.1:p.Thr1387=
XM_011527989.1:c.4125A>C	XP_011526291.1:p.Thr1375=
XM_011527988.2:c.4083A>C	XP_011526290.2:p.Thr1361=
XM_011527989.3:c.4047A>C	XP_011526291.2:p.Thr1349=
NM_000208.4:c.4086A>C MANE Select	NP_000199.2:p.Thr1362=
NM_001079817.3:c.4050A>C	NP_001073285.1:p.Thr1350=