Canonical Allele Identifier: CA1266824955

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551982_85551983delinsCT , CM000664.2:g.85551982_85551983delinsCT	GRCh38
NC_000002.11:g.85779105_85779106delinsCT , CM000664.1:g.85779105_85779106delinsCT	GRCh37
NC_000002.10:g.85632616_85632617delinsCT	NCBI36
NG_011811.2:g.14552_14553delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5916_5917delinsAG
ENST00000482662.2:n.4323_4324delinsAG
ENST00000685865.1:n.2275_2276delinsAG
ENST00000687250.1:n.1975_1976delinsAG
ENST00000687995.1:n.1792-2_1792-1delinsAG
ENST00000688205.1:c.*1033-2_*1033-1delinsAG	ENSP00000509673.1:n.*1033-2_*1033-1delinsAG
ENST00000688788.1:n.1679-2_1679-1delinsAG
ENST00000689276.1:c.1371-2_1371-1delinsAG	ENSP00000510012.1:n.1371-2_1371-1delinsAG
ENST00000689576.1:c.*59-2_*59-1delinsAG	ENSP00000508712.1:n.*59-2_*59-1delinsAG
ENST00000690108.1:c.*1096-2_*1096-1delinsAG	ENSP00000510617.1:n.*1096-2_*1096-1delinsAG
ENST00000690468.1:c.1009-2_1009-1delinsAG	ENSP00000509078.1:n.1009-2_1009-1delinsAG
ENST00000690595.1:c.765-2_765-1delinsAG	ENSP00000508979.1:n.765-2_765-1delinsAG
ENST00000691348.1:c.1117-2_1117-1delinsAG	ENSP00000509369.1:n.1117-2_1117-1delinsAG
ENST00000691410.1:c.*1017-2_*1017-1delinsAG	ENSP00000508479.1:n.*1017-2_*1017-1delinsAG
ENST00000693287.1:c.756-2_756-1delinsAG	ENSP00000510264.1:n.756-2_756-1delinsAG
ENST00000693681.1:c.753-2_753-1delinsAG	ENSP00000510789.1:n.753-2_753-1delinsAG
ENST00000233838.9:c.1440-2_1440-1delinsAG MANE Select	ENSP00000233838.3:n.1440-2_1440-1delinsAG
ENST00000233838.8:c.1440-2_1440-1delinsAG	ENSP00000233838.3:n.1440-2_1440-1delinsAG
ENST00000430215.7:c.1269-2_1269-1delinsAG	ENSP00000408045.3:n.1269-2_1269-1delinsAG
ENST00000465637.5:n.179-3979_179-3978delinsAG
NM_000821.5:c.1440-2_1440-1delinsAG	NP_000812.2:n.1440-2_1440-1delinsAG
NM_000821.6:c.1440-2_1440-1delinsAG	NP_000812.2:n.1440-2_1440-1delinsAG
NM_001142269.2:c.1269-2_1269-1delinsAG	NP_001135741.1:n.1269-2_1269-1delinsAG
NM_001142269.3:c.1269-2_1269-1delinsAG	NP_001135741.1:n.1269-2_1269-1delinsAG
XM_005264259.3:c.1440-2_1440-1delinsAG	XP_005264316.1:n.1440-2_1440-1delinsAG
XM_011532764.1:c.618-2_618-1delinsAG	XP_011531066.1:n.618-2_618-1delinsAG
XM_011532765.1:c.618-2_618-1delinsAG	XP_011531067.1:n.618-2_618-1delinsAG
XR_939677.1:n.1353-2_1353-1delinsAG
XM_005264259.5:c.1440-2_1440-1delinsAG	XP_005264316.1:n.1440-2_1440-1delinsAG
XM_011532764.3:c.618-2_618-1delinsAG	XP_011531066.1:n.618-2_618-1delinsAG
XM_011532765.3:c.618-2_618-1delinsAG	XP_011531067.1:n.618-2_618-1delinsAG
XM_017003803.2:c.1269-2_1269-1delinsAG	XP_016859292.1:n.1269-2_1269-1delinsAG
XR_001738703.2:n.1353-2_1353-1delinsAG
NM_000821.7:c.1440-2_1440-1delinsAG MANE Select	NP_000812.2:n.1440-2_1440-1delinsAG
NM_001142269.4:c.1269-2_1269-1delinsAG	NP_001135741.1:n.1269-2_1269-1delinsAG