Canonical Allele Identifier: CA403669373

Gene: INSR

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3631G>T MANE Select	ENSP00000303830.4:p.Gly1211Trp
ENST00000302850.9:c.3631G>T	ENSP00000303830.4:p.Gly1211Trp
ENST00000341500.9:c.3595G>T	ENSP00000342838.4:p.Gly1199Trp
ENST00000601099.1:n.542G>T
NM_000208.2:c.3631G>T	NP_000199.2:p.Gly1211Trp
NM_000208.3:c.3631G>T	NP_000199.2:p.Gly1211Trp
NM_001079817.1:c.3595G>T	NP_001073285.1:p.Gly1199Trp
NM_001079817.2:c.3595G>T	NP_001073285.1:p.Gly1199Trp
XM_011527988.1:c.3706G>T	XP_011526290.1:p.Gly1236Trp
XM_011527989.1:c.3670G>T	XP_011526291.1:p.Gly1224Trp
XM_011527988.2:c.3628G>T	XP_011526290.2:p.Gly1210Trp
XM_011527989.3:c.3592G>T	XP_011526291.2:p.Gly1198Trp
NM_000208.4:c.3631G>T MANE Select	NP_000199.2:p.Gly1211Trp
NM_001079817.3:c.3595G>T	NP_001073285.1:p.Gly1199Trp