Canonical Allele Identifier: CA1266825487

Gene: GGCX

Linked Data

• dbSNP Id: rs1692046671
• gnomAD v3: 2-85553205-GC-G
• gnomAD v4: 2-85553205-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553206del , CM000664.2:g.85553206del	GRCh38
NC_000002.11:g.85780329del , CM000664.1:g.85780329del	GRCh37
NC_000002.10:g.85633840del	NCBI36
NG_011811.2:g.13329del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5199+26del
ENST00000482662.2:n.3606+26del
ENST00000685865.1:n.1558+26del
ENST00000687250.1:n.1258+26del
ENST00000687995.1:n.1507+26del
ENST00000688205.1:c.*748+26del	ENSP00000509673.1:n.*748+26del
ENST00000688788.1:n.1394+26del
ENST00000689276.1:c.1086+26del	ENSP00000510012.1:n.1086+26del
ENST00000689576.1:c.1155+26del	ENSP00000508712.1:n.1155+26del
ENST00000690108.1:c.*811+26del	ENSP00000510617.1:n.*811+26del
ENST00000690468.1:c.876+26del	ENSP00000509078.1:n.876+26del
ENST00000690595.1:c.480+26del	ENSP00000508979.1:n.480+26del
ENST00000691348.1:c.984+26del	ENSP00000509369.1:n.984+26del
ENST00000691410.1:c.*732+26del	ENSP00000508479.1:n.*732+26del
ENST00000693287.1:c.471+26del	ENSP00000510264.1:n.471+26del
ENST00000693681.1:c.468+26del	ENSP00000510789.1:n.468+26del
ENST00000233838.9:c.1155+26del MANE Select	ENSP00000233838.3:n.1155+26del
ENST00000233838.8:c.1155+26del	ENSP00000233838.3:n.1155+26del
ENST00000430215.7:c.984+26del	ENSP00000408045.3:n.984+26del
ENST00000465637.5:n.179-5202del
ENST00000473665.1:n.648+26del
ENST00000482662.1:n.572+26del
NM_000821.5:c.1155+26del	NP_000812.2:n.1155+26del
NM_000821.6:c.1155+26del	NP_000812.2:n.1155+26del
NM_001142269.2:c.984+26del	NP_001135741.1:n.984+26del
NM_001142269.3:c.984+26del	NP_001135741.1:n.984+26del
XM_005264259.3:c.1155+26del	XP_005264316.1:n.1155+26del
XM_011532764.1:c.333+26del	XP_011531066.1:n.333+26del
XM_011532765.1:c.333+26del	XP_011531067.1:n.333+26del
XR_939677.1:n.1220+26del
XM_005264259.5:c.1155+26del	XP_005264316.1:n.1155+26del
XM_011532764.3:c.333+26del	XP_011531066.1:n.333+26del
XM_011532765.3:c.333+26del	XP_011531067.1:n.333+26del
XM_017003803.2:c.984+26del	XP_016859292.1:n.984+26del
XR_001738703.2:n.1220+26del
NM_000821.7:c.1155+26del MANE Select	NP_000812.2:n.1155+26del
NM_001142269.4:c.984+26del	NP_001135741.1:n.984+26del