Canonical Allele Identifier: CA1682288373

Gene: CYP2W1 C7orf50

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.988812C= , CM000669.2:g.988812C=	GRCh38
NC_000007.13:g.1028448C= , CM000669.1:g.1028448C=	GRCh37
NC_000007.12:g.994974C=	NCBI36
NG_007934.1:g.10614C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308919.12:c.1463C= (CYP2W1) MANE Select	ENSP00000310149.7:p.Pro488=
ENST00000308919.11:c.1463C= (CYP2W1)	ENSP00000310149.7:p.Pro488=
ENST00000340150.10:c.*284C= (CYP2W1)	ENSP00000344178.6:n.*284C=
NM_017781.2:c.1463C= (CYP2W1)	NP_060251.2:p.Pro488=
XM_005249889.3:c.522+8834G= (C7orf50)	XP_005249946.2:n.522+8834G=
XM_011515440.1:c.1358+105C= (CYP2W1)	XP_011513742.1:n.1358+105C=
XM_011515441.1:c.1358+105C= (CYP2W1)	XP_011513743.1:n.1358+105C=
XM_011515580.1:c.1107+8834G= (C7orf50)	XP_011513882.1:n.1107+8834G=
XM_011515581.1:c.564+8834G= (C7orf50)	XP_011513883.1:n.564+8834G=
XM_011515582.1:c.564+8834G= (C7orf50)	XP_011513884.1:n.564+8834G=
XM_011515583.1:c.564+8834G= (C7orf50)	XP_011513885.1:n.564+8834G=
XM_011515584.1:c.564+8834G= (C7orf50)	XP_011513886.1:n.564+8834G=
NR_156697.1:n.547+8834G= (C7orf50)
XM_011515440.3:c.1358+105C= (CYP2W1)	XP_011513742.1:n.1358+105C=
XM_011515441.3:c.1358+105C= (CYP2W1)	XP_011513743.1:n.1358+105C=
XM_011515581.3:c.564+8834G= (C7orf50)	XP_011513883.1:n.564+8834G=
XM_011515582.3:c.564+8834G= (C7orf50)	XP_011513884.1:n.564+8834G=
XM_011515583.2:c.564+8834G= (C7orf50)	XP_011513885.1:n.564+8834G=
XM_011515584.2:c.564+8834G= (C7orf50)	XP_011513886.1:n.564+8834G=
XM_017012719.1:c.1108-3378G= (C7orf50)	XP_016868208.1:n.1108-3378G=
XM_017012720.2:c.564+8834G= (C7orf50)	XP_016868209.1:n.564+8834G=
XM_017012721.2:c.522+8834G= (C7orf50)	XP_016868210.1:n.522+8834G=
NM_017781.3:c.1463C= (CYP2W1) MANE Select	NP_060251.2:p.Pro488=
NR_156697.2:n.547+8834G= (C7orf50)