Canonical Allele Identifier: CA403671200

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125404C>T (hg19) ; chr19:g.7125393C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125393C>T , CM000681.2:g.7125393C>T	GRCh38
NC_000019.9:g.7125404C>T , CM000681.1:g.7125404C>T	GRCh37
NC_000019.8:g.7076404C>T	NCBI36
NG_008852.2:g.173608G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3148G>A MANE Select	ENSP00000303830.4:p.Ala1050Thr
ENST00000302850.9:c.3148G>A	ENSP00000303830.4:p.Ala1050Thr
ENST00000341500.9:c.3112G>A	ENSP00000342838.4:p.Ala1038Thr
NM_000208.2:c.3148G>A	NP_000199.2:p.Ala1050Thr
NM_000208.3:c.3148G>A	NP_000199.2:p.Ala1050Thr
NM_001079817.1:c.3112G>A	NP_001073285.1:p.Ala1038Thr
NM_001079817.2:c.3112G>A	NP_001073285.1:p.Ala1038Thr
XM_011527988.1:c.3223G>A	XP_011526290.1:p.Ala1075Thr
XM_011527989.1:c.3187G>A	XP_011526291.1:p.Ala1063Thr
XM_011527988.2:c.3145G>A	XP_011526290.2:p.Ala1049Thr
XM_011527989.3:c.3109G>A	XP_011526291.2:p.Ala1037Thr
NM_000208.4:c.3148G>A MANE Select	NP_000199.2:p.Ala1050Thr
NM_001079817.3:c.3112G>A	NP_001073285.1:p.Ala1038Thr