Canonical Allele Identifier: CA2581586459

Gene: HCRTR2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55269449T= , CM000668.2:g.55269449T=	GRCh38
NC_000006.11:g.55134247T= , CM000668.1:g.55134247T=	GRCh37
NC_000006.10:g.55242206T=	NCBI36
NG_012447.1:g.100177T=
NG_012447.2:g.167990T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370862.4:c.762+5627T= MANE Select	ENSP00000359899.3:n.762+5627T=
ENST00000370862.3:c.762+5627T=	ENSP00000359899.3:n.762+5627T=
ENST00000615358.4:c.762+5627T=	ENSP00000477548.1:n.762+5627T=
NM_001526.3:c.762+5627T=	NP_001517.2:n.762+5627T=
XM_011514542.1:c.567+5627T=	XP_011512844.1:n.567+5627T=
NM_001526.4:c.762+5627T=	NP_001517.2:n.762+5627T=
XM_017010798.1:c.762+5627T=	XP_016866287.1:n.762+5627T=
NM_001384272.1:c.762+5627T= MANE Select	NP_001371201.1:n.762+5627T=
NM_001526.5:c.762+5627T=	NP_001517.2:n.762+5627T=