Canonical Allele Identifier: CA403668623

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117264C>T (hg19) ; chr19:g.7117253C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117253C>T , CM000681.2:g.7117253C>T	GRCh38
NC_000019.9:g.7117264C>T , CM000681.1:g.7117264C>T	GRCh37
NC_000019.8:g.7068264C>T	NCBI36
NG_008852.2:g.181748G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3952G>A MANE Select	ENSP00000303830.4:p.Glu1318Lys
ENST00000302850.9:c.3952G>A	ENSP00000303830.4:p.Glu1318Lys
ENST00000341500.9:c.3916G>A	ENSP00000342838.4:p.Glu1306Lys
NM_000208.2:c.3952G>A	NP_000199.2:p.Glu1318Lys
NM_000208.3:c.3952G>A	NP_000199.2:p.Glu1318Lys
NM_001079817.1:c.3916G>A	NP_001073285.1:p.Glu1306Lys
NM_001079817.2:c.3916G>A	NP_001073285.1:p.Glu1306Lys
XM_011527988.1:c.4027G>A	XP_011526290.1:p.Glu1343Lys
XM_011527989.1:c.3991G>A	XP_011526291.1:p.Glu1331Lys
XM_011527988.2:c.3949G>A	XP_011526290.2:p.Glu1317Lys
XM_011527989.3:c.3913G>A	XP_011526291.2:p.Glu1305Lys
NM_000208.4:c.3952G>A MANE Select	NP_000199.2:p.Glu1318Lys
NM_001079817.3:c.3916G>A	NP_001073285.1:p.Glu1306Lys