Canonical Allele Identifier: CA505216060

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117085A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117074A>G , CM000681.2:g.7117074A>G	GRCh38
NC_000019.9:g.7117085A>G , CM000681.1:g.7117085A>G	GRCh37
NC_000019.8:g.7068085A>G	NCBI36
NG_008852.2:g.181927T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4131T>C MANE Select	ENSP00000303830.4:p.Pro1377=
ENST00000302850.9:c.4131T>C	ENSP00000303830.4:p.Pro1377=
ENST00000341500.9:c.4095T>C	ENSP00000342838.4:p.Pro1365=
NM_000208.2:c.4131T>C	NP_000199.2:p.Pro1377=
NM_000208.3:c.4131T>C	NP_000199.2:p.Pro1377=
NM_001079817.1:c.4095T>C	NP_001073285.1:p.Pro1365=
NM_001079817.2:c.4095T>C	NP_001073285.1:p.Pro1365=
XM_011527988.1:c.4206T>C	XP_011526290.1:p.Pro1402=
XM_011527989.1:c.4170T>C	XP_011526291.1:p.Pro1390=
XM_011527988.2:c.4128T>C	XP_011526290.2:p.Pro1376=
XM_011527989.3:c.4092T>C	XP_011526291.2:p.Pro1364=
NM_000208.4:c.4131T>C MANE Select	NP_000199.2:p.Pro1377=
NM_001079817.3:c.4095T>C	NP_001073285.1:p.Pro1365=