Canonical Allele Identifier: CA2681379314

Gene: C7orf50

Linked Data

• gnomAD v4: 7-983118-GGTGGGGTGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.983120_983128del , CM000669.2:g.983120_983128del	GRCh38
NC_000007.13:g.1022756_1022764del , CM000669.1:g.1022756_1022764del	GRCh37
NC_000007.12:g.989282_989290del	NCBI36
NG_007934.1:g.4922_4930del

Transcript Alleles

HGVS	Amino-acid Change
XM_005249889.3:c.523-4066_523-4058del	XP_005249946.2:n.523-4066_523-4058del
XM_011515580.1:c.1108-4066_1108-4058del	XP_011513882.1:n.1108-4066_1108-4058del
XM_011515581.1:c.565-4066_565-4058del	XP_011513883.1:n.565-4066_565-4058del
XM_011515582.1:c.565-4066_565-4058del	XP_011513884.1:n.565-4066_565-4058del
XM_011515583.1:c.565-4066_565-4058del	XP_011513885.1:n.565-4066_565-4058del
XM_011515584.1:c.565-4066_565-4058del	XP_011513886.1:n.565-4066_565-4058del
NR_156697.1:n.548-4066_548-4058del
XM_011515581.3:c.565-4066_565-4058del	XP_011513883.1:n.565-4066_565-4058del
XM_011515582.3:c.565-4066_565-4058del	XP_011513884.1:n.565-4066_565-4058del
XM_011515583.2:c.565-4066_565-4058del	XP_011513885.1:n.565-4066_565-4058del
XM_011515584.2:c.565-4066_565-4058del	XP_011513886.1:n.565-4066_565-4058del
XM_017012720.2:c.565-4066_565-4058del	XP_016868209.1:n.565-4066_565-4058del
XM_017012721.2:c.523-4066_523-4058del	XP_016868210.1:n.523-4066_523-4058del
NR_156697.2:n.548-4066_548-4058del