Canonical Allele Identifier: CA1260374697

Gene: CYP26B1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.72134831A= , CM000664.2:g.72134831A=	GRCh38
NC_000002.11:g.72361960A= , CM000664.1:g.72361960A=	GRCh37
NC_000002.10:g.72215468A=	NCBI36
NG_007957.1:g.18004T=

Transcript Alleles

HGVS	Amino-acid Change
NM_019885.4:c.791T= MANE Select	NP_063938.1:p.Leu264=
ENST00000001146.7:c.791T= MANE Select	ENSP00000001146.2:p.Leu264=
NM_001277742.1:c.566T=	NP_001264671.1:p.Leu189=
NM_001277742.2:c.566T=	NP_001264671.1:p.Leu189=
NM_019885.3:c.791T=	NP_063938.1:p.Leu264=
ENST00000001146.6:c.791T=	ENSP00000001146.2:p.Leu264=
ENST00000412253.1:c.218T=	ENSP00000401465.1:p.Leu73=
ENST00000546307.5:c.566T=	ENSP00000443304.1:p.Leu189=
XM_005264433.3:c.617T=	XP_005264490.1:p.Leu206=
XM_005264433.4:c.617T=	XP_005264490.1:p.Leu206=
XM_011532988.1:c.218T=	XP_011531290.1:p.Leu73=