Canonical Allele Identifier: CA1139925488

Gene: HCRTR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.31626924A= , CM000663.2:g.31626924A=	GRCh38
NC_000001.10:g.32092525A= , CM000663.1:g.32092525A=	GRCh37
NC_000001.9:g.31865112A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403528.7:c.1222A= MANE Select	ENSP00000384387.2:p.Ile408=
ENST00000686354.1:n.1375A=
ENST00000373705.1:c.1087+1806A=	ENSP00000362809.1:n.1087+1806A=
ENST00000373706.9:c.1222A=	ENSP00000362810.5:p.Ile408=
ENST00000403528.6:c.1222A=	ENSP00000384387.2:p.Ile408=
ENST00000468521.1:n.1414-399A=
NM_001525.2:c.1222A=	NP_001516.2:p.Ile408=
XM_011541308.1:c.1222A=	XP_011539610.1:p.Ile408=
XM_017001107.1:c.1087+1806A=	XP_016856596.1:n.1087+1806A=
XM_024446602.1:c.1222A=	XP_024302370.1:p.Ile408=
XM_024446603.1:c.1222A=	XP_024302371.1:p.Ile408=
XM_024446604.1:c.1222A=	XP_024302372.1:p.Ile408=
XM_024446605.1:c.1222A=	XP_024302373.1:p.Ile408=
NM_001525.3:c.1222A= MANE Select	NP_001516.2:p.Ile408=