Canonical Allele Identifier: CA1682306408

Gene: CYP2W1 C7orf50

Linked Data

• dbSNP Id: rs1848071264

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.983387_983396del , CM000669.2:g.983387_983396del	GRCh38
NC_000007.13:g.1023023_1023032del , CM000669.1:g.1023023_1023032del	GRCh37
NC_000007.12:g.989549_989558del	NCBI36
NG_007934.1:g.5189_5198del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308919.12:c.174+2_174+11del (CYP2W1)
ENST00000308919.11:c.174+2_174+11del (CYP2W1)
ENST00000340150.10:c.6+2_6+11del (CYP2W1)
NM_017781.2:c.174+2_174+11del (CYP2W1)
XM_005249889.3:c.523-4333_523-4324del (C7orf50)	XP_005249946.2:n.523-4333_523-4324del
XM_011515440.1:c.174+2_174+11del (CYP2W1)
XM_011515441.1:c.174+2_174+11del (CYP2W1)
XM_011515580.1:c.1108-4333_1108-4324del (C7orf50)	XP_011513882.1:n.1108-4333_1108-4324del
XM_011515581.1:c.565-4333_565-4324del (C7orf50)	XP_011513883.1:n.565-4333_565-4324del
XM_011515582.1:c.565-4333_565-4324del (C7orf50)	XP_011513884.1:n.565-4333_565-4324del
XM_011515583.1:c.565-4333_565-4324del (C7orf50)	XP_011513885.1:n.565-4333_565-4324del
XM_011515584.1:c.565-4333_565-4324del (C7orf50)	XP_011513886.1:n.565-4333_565-4324del
NR_156697.1:n.548-4333_548-4324del (C7orf50)
XM_011515440.3:c.174+2_174+11del (CYP2W1)
XM_011515441.3:c.174+2_174+11del (CYP2W1)
XM_011515581.3:c.565-4333_565-4324del (C7orf50)	XP_011513883.1:n.565-4333_565-4324del
XM_011515582.3:c.565-4333_565-4324del (C7orf50)	XP_011513884.1:n.565-4333_565-4324del
XM_011515583.2:c.565-4333_565-4324del (C7orf50)	XP_011513885.1:n.565-4333_565-4324del
XM_011515584.2:c.565-4333_565-4324del (C7orf50)	XP_011513886.1:n.565-4333_565-4324del
XM_017012720.2:c.565-4333_565-4324del (C7orf50)	XP_016868209.1:n.565-4333_565-4324del
XM_017012721.2:c.523-4333_523-4324del (C7orf50)	XP_016868210.1:n.523-4333_523-4324del
NM_017781.3:c.174+2_174+11del (CYP2W1)
NR_156697.2:n.548-4333_548-4324del (C7orf50)