Canonical Allele Identifier: CA2577020944

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553509G>C , CM000664.2:g.85553509G>C	GRCh38
NC_000002.11:g.85780632G>C , CM000664.1:g.85780632G>C	GRCh37
NC_000002.10:g.85634143G>C	NCBI36
NG_011811.2:g.13026C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000473665.2:n.4934-12C>G
ENST00000482662.2:n.3329C>G
ENST00000685865.1:n.1293-12C>G
ENST00000687250.1:n.993-12C>G
ENST00000687995.1:n.1242-12C>G
ENST00000688205.1:c.*483-12C>G	ENSP00000509673.1:n.*483-12C>G
ENST00000688788.1:n.1129-12C>G
ENST00000689276.1:c.821-12C>G	ENSP00000510012.1:n.821-12C>G
ENST00000689576.1:c.890-12C>G	ENSP00000508712.1:n.890-12C>G
ENST00000690108.1:c.*546-12C>G	ENSP00000510617.1:n.*546-12C>G
ENST00000690468.1:c.611-12C>G	ENSP00000509078.1:n.611-12C>G
ENST00000690595.1:c.215-12C>G	ENSP00000508979.1:n.215-12C>G
ENST00000691348.1:c.719-12C>G	ENSP00000509369.1:n.719-12C>G
ENST00000691410.1:c.*467-12C>G	ENSP00000508479.1:n.*467-12C>G
ENST00000693287.1:c.206-12C>G	ENSP00000510264.1:n.206-12C>G
ENST00000693681.1:c.203-12C>G	ENSP00000510789.1:n.203-12C>G
ENST00000233838.9:c.890-12C>G MANE Select	ENSP00000233838.3:n.890-12C>G
ENST00000233838.8:c.890-12C>G	ENSP00000233838.3:n.890-12C>G
ENST00000430215.7:c.719-12C>G	ENSP00000408045.3:n.719-12C>G
ENST00000465637.5:n.178+5497C>G
ENST00000473665.1:n.383-12C>G
ENST00000482662.1:n.295C>G
NM_000821.5:c.890-12C>G	NP_000812.2:n.890-12C>G
NM_000821.6:c.890-12C>G	NP_000812.2:n.890-12C>G
NM_001142269.2:c.719-12C>G	NP_001135741.1:n.719-12C>G
NM_001142269.3:c.719-12C>G	NP_001135741.1:n.719-12C>G
XM_005264259.3:c.890-12C>G	XP_005264316.1:n.890-12C>G
XM_011532764.1:c.68-12C>G	XP_011531066.1:n.68-12C>G
XM_011532765.1:c.68-12C>G	XP_011531067.1:n.68-12C>G
XR_939677.1:n.955-12C>G
XM_005264259.5:c.890-12C>G	XP_005264316.1:n.890-12C>G
XM_011532764.3:c.68-12C>G	XP_011531066.1:n.68-12C>G
XM_011532765.3:c.68-12C>G	XP_011531067.1:n.68-12C>G
XM_017003803.2:c.719-12C>G	XP_016859292.1:n.719-12C>G
XR_001738703.2:n.955-12C>G
NM_000821.7:c.890-12C>G MANE Select	NP_000812.2:n.890-12C>G
NM_001142269.4:c.719-12C>G	NP_001135741.1:n.719-12C>G