Canonical Allele Identifier: CA366536832

Gene: C7orf50 CYP2W1

Linked Data

• dbSNP Id: rs1554282112
• gnomAD v2: 7-1022797-CG-C
• gnomAD v3: 7-983161-CG-C
• gnomAD v4: 7-983161-CG-C
• MyVariant Identifiers: chr7:g.1022798del (hg19) ; chr7:g.983163del (hg38) ; chr7:g.983162del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.983168del , CM000669.2:g.983168del	GRCh38
NC_000007.13:g.1022804del , CM000669.1:g.1022804del	GRCh37
NC_000007.12:g.989330del	NCBI36
NG_007934.1:g.4970del

Transcript Alleles

HGVS	Amino-acid Change
XM_005249889.3:c.523-4101del (C7orf50)	XP_005249946.2:n.523-4101del
XM_011515440.1:c.-44del (CYP2W1)	XP_011513742.1:n.-44del
XM_011515441.1:c.-44del (CYP2W1)	XP_011513743.1:n.-44del
XM_011515580.1:c.1108-4101del (C7orf50)	XP_011513882.1:n.1108-4101del
XM_011515581.1:c.565-4101del (C7orf50)	XP_011513883.1:n.565-4101del
XM_011515582.1:c.565-4101del (C7orf50)	XP_011513884.1:n.565-4101del
XM_011515583.1:c.565-4101del (C7orf50)	XP_011513885.1:n.565-4101del
XM_011515584.1:c.565-4101del (C7orf50)	XP_011513886.1:n.565-4101del
NR_156697.1:n.548-4101del (C7orf50)
XM_011515440.3:c.-44del (CYP2W1)	XP_011513742.1:n.-44del
XM_011515441.3:c.-44del (CYP2W1)	XP_011513743.1:n.-44del
XM_011515581.3:c.565-4101del (C7orf50)	XP_011513883.1:n.565-4101del
XM_011515582.3:c.565-4101del (C7orf50)	XP_011513884.1:n.565-4101del
XM_011515583.2:c.565-4101del (C7orf50)	XP_011513885.1:n.565-4101del
XM_011515584.2:c.565-4101del (C7orf50)	XP_011513886.1:n.565-4101del
XM_017012720.2:c.565-4101del (C7orf50)	XP_016868209.1:n.565-4101del
XM_017012721.2:c.523-4101del (C7orf50)	XP_016868210.1:n.523-4101del
NR_156697.2:n.548-4101del (C7orf50)