Canonical Allele Identifier: CA1266825393

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553009_85553010delinsCG , CM000664.2:g.85553009_85553010delinsCG	GRCh38
NC_000002.11:g.85780132_85780133delinsCG , CM000664.1:g.85780132_85780133delinsCG	GRCh37
NC_000002.10:g.85633643_85633644delinsCG	NCBI36
NG_011811.2:g.13525_13526delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5260_5261delinsCG
ENST00000482662.2:n.3667_3668delinsCG
ENST00000685865.1:n.1619_1620delinsCG
ENST00000687250.1:n.1319_1320delinsCG
ENST00000687995.1:n.1568_1569delinsCG
ENST00000688205.1:c.*809_*810delinsCG	ENSP00000509673.1:n.*809_*810delinsCG
ENST00000688788.1:n.1455_1456delinsCG
ENST00000689276.1:c.1147_1148delinsCG	ENSP00000510012.1:p.Arg383=
ENST00000689576.1:c.1216_1217delinsCG	ENSP00000508712.1:p.Arg406=
ENST00000690108.1:c.*872_*873delinsCG	ENSP00000510617.1:n.*872_*873delinsCG
ENST00000690468.1:c.937_938delinsCG	ENSP00000509078.1:p.Arg313=
ENST00000690595.1:c.541_542delinsCG	ENSP00000508979.1:p.Arg181=
ENST00000691348.1:c.1045_1046delinsCG	ENSP00000509369.1:p.Arg349=
ENST00000691410.1:c.*793_*794delinsCG	ENSP00000508479.1:n.*793_*794delinsCG
ENST00000693287.1:c.532_533delinsCG	ENSP00000510264.1:p.Arg178=
ENST00000693681.1:c.529_530delinsCG	ENSP00000510789.1:p.Arg177=
ENST00000233838.9:c.1216_1217delinsCG MANE Select	ENSP00000233838.3:p.Arg406=
ENST00000233838.8:c.1216_1217delinsCG	ENSP00000233838.3:p.Arg406=
ENST00000430215.7:c.1045_1046delinsCG	ENSP00000408045.3:p.Arg349=
ENST00000465637.5:n.179-5006_179-5005delinsCG
ENST00000473665.1:n.709_710delinsCG
ENST00000482662.1:n.633_634delinsCG
NM_000821.5:c.1216_1217delinsCG	NP_000812.2:p.Arg406=
NM_000821.6:c.1216_1217delinsCG	NP_000812.2:p.Arg406=
NM_001142269.2:c.1045_1046delinsCG	NP_001135741.1:p.Arg349=
NM_001142269.3:c.1045_1046delinsCG	NP_001135741.1:p.Arg349=
XM_005264259.3:c.1216_1217delinsCG	XP_005264316.1:p.Arg406=
XM_011532764.1:c.394_395delinsCG	XP_011531066.1:p.Arg132=
XM_011532765.1:c.394_395delinsCG	XP_011531067.1:p.Arg132=
XR_939677.1:n.1281_1282delinsCG
XM_005264259.5:c.1216_1217delinsCG	XP_005264316.1:p.Arg406=
XM_011532764.3:c.394_395delinsCG	XP_011531066.1:p.Arg132=
XM_011532765.3:c.394_395delinsCG	XP_011531067.1:p.Arg132=
XM_017003803.2:c.1045_1046delinsCG	XP_016859292.1:p.Arg349=
XR_001738703.2:n.1281_1282delinsCG
NM_000821.7:c.1216_1217delinsCG MANE Select	NP_000812.2:p.Arg406=
NM_001142269.4:c.1045_1046delinsCG	NP_001135741.1:p.Arg349=