Canonical Allele Identifier: CA403669371

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7120658C>T (hg19) ; chr19:g.7120647C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120647C>T , CM000681.2:g.7120647C>T	GRCh38
NC_000019.9:g.7120658C>T , CM000681.1:g.7120658C>T	GRCh37
NC_000019.8:g.7071658C>T	NCBI36
NG_008852.2:g.178354G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3632G>A MANE Select	ENSP00000303830.4:p.Gly1211Glu
ENST00000302850.9:c.3632G>A	ENSP00000303830.4:p.Gly1211Glu
ENST00000341500.9:c.3596G>A	ENSP00000342838.4:p.Gly1199Glu
ENST00000601099.1:n.543G>A
NM_000208.2:c.3632G>A	NP_000199.2:p.Gly1211Glu
NM_000208.3:c.3632G>A	NP_000199.2:p.Gly1211Glu
NM_001079817.1:c.3596G>A	NP_001073285.1:p.Gly1199Glu
NM_001079817.2:c.3596G>A	NP_001073285.1:p.Gly1199Glu
XM_011527988.1:c.3707G>A	XP_011526290.1:p.Gly1236Glu
XM_011527989.1:c.3671G>A	XP_011526291.1:p.Gly1224Glu
XM_011527988.2:c.3629G>A	XP_011526290.2:p.Gly1210Glu
XM_011527989.3:c.3593G>A	XP_011526291.2:p.Gly1198Glu
NM_000208.4:c.3632G>A MANE Select	NP_000199.2:p.Gly1211Glu
NM_001079817.3:c.3596G>A	NP_001073285.1:p.Gly1199Glu