Canonical Allele Identifier: CA403668547

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117234G>T (hg19) ; chr19:g.7117223G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117223G>T , CM000681.2:g.7117223G>T	GRCh38
NC_000019.9:g.7117234G>T , CM000681.1:g.7117234G>T	GRCh37
NC_000019.8:g.7068234G>T	NCBI36
NG_008852.2:g.181778C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3982C>A MANE Select	ENSP00000303830.4:p.Pro1328Thr
ENST00000302850.9:c.3982C>A	ENSP00000303830.4:p.Pro1328Thr
ENST00000341500.9:c.3946C>A	ENSP00000342838.4:p.Pro1316Thr
NM_000208.2:c.3982C>A	NP_000199.2:p.Pro1328Thr
NM_000208.3:c.3982C>A	NP_000199.2:p.Pro1328Thr
NM_001079817.1:c.3946C>A	NP_001073285.1:p.Pro1316Thr
NM_001079817.2:c.3946C>A	NP_001073285.1:p.Pro1316Thr
XM_011527988.1:c.4057C>A	XP_011526290.1:p.Pro1353Thr
XM_011527989.1:c.4021C>A	XP_011526291.1:p.Pro1341Thr
XM_011527988.2:c.3979C>A	XP_011526290.2:p.Pro1327Thr
XM_011527989.3:c.3943C>A	XP_011526291.2:p.Pro1315Thr
NM_000208.4:c.3982C>A MANE Select	NP_000199.2:p.Pro1328Thr
NM_001079817.3:c.3946C>A	NP_001073285.1:p.Pro1316Thr