Canonical Allele Identifier: CA403668709

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117301G>T (hg19) ; chr19:g.7117290G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117290G>T , CM000681.2:g.7117290G>T	GRCh38
NC_000019.9:g.7117301G>T , CM000681.1:g.7117301G>T	GRCh37
NC_000019.8:g.7068301G>T	NCBI36
NG_008852.2:g.181711C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3915C>A MANE Select	ENSP00000303830.4:p.His1305Gln
ENST00000302850.9:c.3915C>A	ENSP00000303830.4:p.His1305Gln
ENST00000341500.9:c.3879C>A	ENSP00000342838.4:p.His1293Gln
NM_000208.2:c.3915C>A	NP_000199.2:p.His1305Gln
NM_000208.3:c.3915C>A	NP_000199.2:p.His1305Gln
NM_001079817.1:c.3879C>A	NP_001073285.1:p.His1293Gln
NM_001079817.2:c.3879C>A	NP_001073285.1:p.His1293Gln
XM_011527988.1:c.3990C>A	XP_011526290.1:p.His1330Gln
XM_011527989.1:c.3954C>A	XP_011526291.1:p.His1318Gln
XM_011527988.2:c.3912C>A	XP_011526290.2:p.His1304Gln
XM_011527989.3:c.3876C>A	XP_011526291.2:p.His1292Gln
NM_000208.4:c.3915C>A MANE Select	NP_000199.2:p.His1305Gln
NM_001079817.3:c.3879C>A	NP_001073285.1:p.His1293Gln