Canonical Allele Identifier: CA1266825486

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553205_85553206delinsGC , CM000664.2:g.85553205_85553206delinsGC	GRCh38
NC_000002.11:g.85780328_85780329delinsGC , CM000664.1:g.85780328_85780329delinsGC	GRCh37
NC_000002.10:g.85633839_85633840delinsGC	NCBI36
NG_011811.2:g.13329_13330delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5199+26_5199+27delinsGC
ENST00000482662.2:n.3606+26_3606+27delinsGC
ENST00000685865.1:n.1558+26_1558+27delinsGC
ENST00000687250.1:n.1258+26_1258+27delinsGC
ENST00000687995.1:n.1507+26_1507+27delinsGC
ENST00000688205.1:c.*748+26_*748+27delinsGC	ENSP00000509673.1:n.*748+26_*748+27delinsGC
ENST00000688788.1:n.1394+26_1394+27delinsGC
ENST00000689276.1:c.1086+26_1086+27delinsGC	ENSP00000510012.1:n.1086+26_1086+27delinsGC
ENST00000689576.1:c.1155+26_1155+27delinsGC	ENSP00000508712.1:n.1155+26_1155+27delinsGC
ENST00000690108.1:c.*811+26_*811+27delinsGC	ENSP00000510617.1:n.*811+26_*811+27delinsGC
ENST00000690468.1:c.876+26_876+27delinsGC	ENSP00000509078.1:n.876+26_876+27delinsGC
ENST00000690595.1:c.480+26_480+27delinsGC	ENSP00000508979.1:n.480+26_480+27delinsGC
ENST00000691348.1:c.984+26_984+27delinsGC	ENSP00000509369.1:n.984+26_984+27delinsGC
ENST00000691410.1:c.*732+26_*732+27delinsGC	ENSP00000508479.1:n.*732+26_*732+27delinsGC
ENST00000693287.1:c.471+26_471+27delinsGC	ENSP00000510264.1:n.471+26_471+27delinsGC
ENST00000693681.1:c.468+26_468+27delinsGC	ENSP00000510789.1:n.468+26_468+27delinsGC
ENST00000233838.9:c.1155+26_1155+27delinsGC MANE Select	ENSP00000233838.3:n.1155+26_1155+27delinsGC
ENST00000233838.8:c.1155+26_1155+27delinsGC	ENSP00000233838.3:n.1155+26_1155+27delinsGC
ENST00000430215.7:c.984+26_984+27delinsGC	ENSP00000408045.3:n.984+26_984+27delinsGC
ENST00000465637.5:n.179-5202_179-5201delinsGC
ENST00000473665.1:n.648+26_648+27delinsGC
ENST00000482662.1:n.572+26_572+27delinsGC
NM_000821.5:c.1155+26_1155+27delinsGC	NP_000812.2:n.1155+26_1155+27delinsGC
NM_000821.6:c.1155+26_1155+27delinsGC	NP_000812.2:n.1155+26_1155+27delinsGC
NM_001142269.2:c.984+26_984+27delinsGC	NP_001135741.1:n.984+26_984+27delinsGC
NM_001142269.3:c.984+26_984+27delinsGC	NP_001135741.1:n.984+26_984+27delinsGC
XM_005264259.3:c.1155+26_1155+27delinsGC	XP_005264316.1:n.1155+26_1155+27delinsGC
XM_011532764.1:c.333+26_333+27delinsGC	XP_011531066.1:n.333+26_333+27delinsGC
XM_011532765.1:c.333+26_333+27delinsGC	XP_011531067.1:n.333+26_333+27delinsGC
XR_939677.1:n.1220+26_1220+27delinsGC
XM_005264259.5:c.1155+26_1155+27delinsGC	XP_005264316.1:n.1155+26_1155+27delinsGC
XM_011532764.3:c.333+26_333+27delinsGC	XP_011531066.1:n.333+26_333+27delinsGC
XM_011532765.3:c.333+26_333+27delinsGC	XP_011531067.1:n.333+26_333+27delinsGC
XM_017003803.2:c.984+26_984+27delinsGC	XP_016859292.1:n.984+26_984+27delinsGC
XR_001738703.2:n.1220+26_1220+27delinsGC
NM_000821.7:c.1155+26_1155+27delinsGC MANE Select	NP_000812.2:n.1155+26_1155+27delinsGC
NM_001142269.4:c.984+26_984+27delinsGC	NP_001135741.1:n.984+26_984+27delinsGC