Canonical Allele Identifier: CA2659852720

Gene: GGCX

Linked Data

• gnomAD v4: 2-85551779-GAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551781_85551782del , CM000664.2:g.85551781_85551782del	GRCh38
NC_000002.11:g.85778904_85778905del , CM000664.1:g.85778904_85778905del	GRCh37
NC_000002.10:g.85632415_85632416del	NCBI36
NG_011811.2:g.14754_14755del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.6087+31_6087+32del
ENST00000482662.2:n.4494+31_4494+32del
ENST00000685865.1:n.2477_2478del
ENST00000687250.1:n.2146+31_2146+32del
ENST00000687995.1:n.1961+31_1961+32del
ENST00000688205.1:c.*1202+31_*1202+32del	ENSP00000509673.1:n.*1202+31_*1202+32del
ENST00000688788.1:n.1848+31_1848+32del
ENST00000689276.1:c.1540+31_1540+32del	ENSP00000510012.1:n.1540+31_1540+32del
ENST00000689576.1:c.*228+31_*228+32del	ENSP00000508712.1:n.*228+31_*228+32del
ENST00000690108.1:c.*1265+31_*1265+32del	ENSP00000510617.1:n.*1265+31_*1265+32del
ENST00000690468.1:c.*161+31_*161+32del	ENSP00000509078.1:n.*161+31_*161+32del
ENST00000690595.1:c.934+31_934+32del	ENSP00000508979.1:n.934+31_934+32del
ENST00000691348.1:c.*161+31_*161+32del	ENSP00000509369.1:n.*161+31_*161+32del
ENST00000691410.1:c.*1186+31_*1186+32del	ENSP00000508479.1:n.*1186+31_*1186+32del
ENST00000693287.1:c.925+31_925+32del	ENSP00000510264.1:n.925+31_925+32del
ENST00000693681.1:c.922+31_922+32del	ENSP00000510789.1:n.922+31_922+32del
ENST00000233838.9:c.1609+31_1609+32del MANE Select	ENSP00000233838.3:n.1609+31_1609+32del
ENST00000233838.8:c.1609+31_1609+32del	ENSP00000233838.3:n.1609+31_1609+32del
ENST00000430215.7:c.1438+31_1438+32del	ENSP00000408045.3:n.1438+31_1438+32del
ENST00000465637.5:n.179-3777_179-3776del
NM_000821.5:c.1609+31_1609+32del	NP_000812.2:n.1609+31_1609+32del
NM_000821.6:c.1609+31_1609+32del	NP_000812.2:n.1609+31_1609+32del
NM_001142269.2:c.1438+31_1438+32del	NP_001135741.1:n.1438+31_1438+32del
NM_001142269.3:c.1438+31_1438+32del	NP_001135741.1:n.1438+31_1438+32del
XM_005264259.3:c.1609+31_1609+32del	XP_005264316.1:n.1609+31_1609+32del
XM_011532764.1:c.787+31_787+32del	XP_011531066.1:n.787+31_787+32del
XM_011532765.1:c.787+31_787+32del	XP_011531067.1:n.787+31_787+32del
XR_939677.1:n.1522+31_1522+32del
XM_005264259.5:c.1609+31_1609+32del	XP_005264316.1:n.1609+31_1609+32del
XM_011532764.3:c.787+31_787+32del	XP_011531066.1:n.787+31_787+32del
XM_011532765.3:c.787+31_787+32del	XP_011531067.1:n.787+31_787+32del
XM_017003803.2:c.1438+31_1438+32del	XP_016859292.1:n.1438+31_1438+32del
XR_001738703.2:n.1522+31_1522+32del
NM_000821.7:c.1609+31_1609+32del MANE Select	NP_000812.2:n.1609+31_1609+32del
NM_001142269.4:c.1438+31_1438+32del	NP_001135741.1:n.1438+31_1438+32del