Canonical Allele Identifier: CA403669374

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7120659C>G (hg19) ; chr19:g.7120648C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120648C>G , CM000681.2:g.7120648C>G	GRCh38
NC_000019.9:g.7120659C>G , CM000681.1:g.7120659C>G	GRCh37
NC_000019.8:g.7071659C>G	NCBI36
NG_008852.2:g.178353G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3631G>C MANE Select	ENSP00000303830.4:p.Gly1211Arg
ENST00000302850.9:c.3631G>C	ENSP00000303830.4:p.Gly1211Arg
ENST00000341500.9:c.3595G>C	ENSP00000342838.4:p.Gly1199Arg
ENST00000601099.1:n.542G>C
NM_000208.2:c.3631G>C	NP_000199.2:p.Gly1211Arg
NM_000208.3:c.3631G>C	NP_000199.2:p.Gly1211Arg
NM_001079817.1:c.3595G>C	NP_001073285.1:p.Gly1199Arg
NM_001079817.2:c.3595G>C	NP_001073285.1:p.Gly1199Arg
XM_011527988.1:c.3706G>C	XP_011526290.1:p.Gly1236Arg
XM_011527989.1:c.3670G>C	XP_011526291.1:p.Gly1224Arg
XM_011527988.2:c.3628G>C	XP_011526290.2:p.Gly1210Arg
XM_011527989.3:c.3592G>C	XP_011526291.2:p.Gly1198Arg
NM_000208.4:c.3631G>C MANE Select	NP_000199.2:p.Gly1211Arg
NM_001079817.3:c.3595G>C	NP_001073285.1:p.Gly1199Arg