Canonical Allele Identifier: CA2659852941

Gene: GGCX

Linked Data

• gnomAD v4: 2-85551980-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551982del , CM000664.2:g.85551982del	GRCh38
NC_000002.11:g.85779105del , CM000664.1:g.85779105del	GRCh37
NC_000002.10:g.85632616del	NCBI36
NG_011811.2:g.14554del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5918del
ENST00000482662.2:n.4325del
ENST00000685865.1:n.2277del
ENST00000687250.1:n.1977del
ENST00000687995.1:n.1792del
ENST00000688205.1:c.*1033del
ENST00000688788.1:n.1679del
ENST00000689276.1:c.1371del
ENST00000689576.1:c.*59del
ENST00000690108.1:c.*1096del
ENST00000690468.1:c.1009del
ENST00000690595.1:c.765del
ENST00000691348.1:c.1117del
ENST00000691410.1:c.*1017del
ENST00000693287.1:c.756del
ENST00000693681.1:c.753del
ENST00000233838.9:c.1440del
ENST00000233838.8:c.1440del
ENST00000430215.7:c.1269del
ENST00000465637.5:n.179-3977del
NM_000821.5:c.1440del
NM_000821.6:c.1440del
NM_001142269.2:c.1269del
NM_001142269.3:c.1269del
XM_005264259.3:c.1440del
XM_011532764.1:c.618del
XM_011532765.1:c.618del
XR_939677.1:n.1353del
XM_005264259.5:c.1440del
XM_011532764.3:c.618del
XM_011532765.3:c.618del
XM_017003803.2:c.1269del
XR_001738703.2:n.1353del
NM_000821.7:c.1440del
NM_001142269.4:c.1269del