Canonical Allele Identifier: CA1266825555

Gene: GGCX

Linked Data

• dbSNP Id: rs758998960

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553382_85553394dup , CM000664.2:g.85553382_85553394dup	GRCh38
NC_000002.11:g.85780505_85780517dup , CM000664.1:g.85780505_85780517dup	GRCh37
NC_000002.10:g.85634016_85634028dup	NCBI36
NG_011811.2:g.13149_13161dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000473665.2:n.5045_5057dup
ENST00000482662.2:n.3452_3464dup
ENST00000685865.1:n.1404_1416dup
ENST00000687250.1:n.1104_1116dup
ENST00000687995.1:n.1353_1365dup
ENST00000688205.1:c.*594_*606dup	ENSP00000509673.1:n.*594_*606dup
ENST00000688788.1:n.1240_1252dup
ENST00000689276.1:c.932_944dup	ENSP00000510012.1:p.Pro316GlyfsTer12
ENST00000689576.1:c.1001_1013dup	ENSP00000508712.1:p.Pro339GlyfsTer12
ENST00000690108.1:c.*657_*669dup	ENSP00000510617.1:n.*657_*669dup
ENST00000690468.1:c.722_734dup	ENSP00000509078.1:p.Pro246GlyfsTer12
ENST00000690595.1:c.326_338dup	ENSP00000508979.1:p.Pro114GlyfsTer12
ENST00000691348.1:c.830_842dup	ENSP00000509369.1:p.Pro282GlyfsTer12
ENST00000691410.1:c.*578_*590dup	ENSP00000508479.1:n.*578_*590dup
ENST00000693287.1:c.317_329dup	ENSP00000510264.1:p.Pro111GlyfsTer12
ENST00000693681.1:c.314_326dup	ENSP00000510789.1:p.Pro110GlyfsTer12
ENST00000233838.9:c.1001_1013dup MANE Select	ENSP00000233838.3:p.Pro339GlyfsTer12
ENST00000233838.8:c.1001_1013dup	ENSP00000233838.3:p.Pro339GlyfsTer12
ENST00000430215.7:c.830_842dup	ENSP00000408045.3:p.Pro282GlyfsTer12
ENST00000465637.5:n.179-5382_179-5370dup
ENST00000473665.1:n.494_506dup
ENST00000482662.1:n.418_430dup
NM_000821.5:c.1001_1013dup	NP_000812.2:p.Pro339GlyfsTer12
NM_000821.6:c.1001_1013dup	NP_000812.2:p.Pro339GlyfsTer12
NM_001142269.2:c.830_842dup	NP_001135741.1:p.Pro282GlyfsTer12
NM_001142269.3:c.830_842dup	NP_001135741.1:p.Pro282GlyfsTer12
XM_005264259.3:c.1001_1013dup	XP_005264316.1:p.Pro339GlyfsTer12
XM_011532764.1:c.179_191dup	XP_011531066.1:p.Pro65GlyfsTer12
XM_011532765.1:c.179_191dup	XP_011531067.1:p.Pro65GlyfsTer12
XR_939677.1:n.1066_1078dup
XM_005264259.5:c.1001_1013dup	XP_005264316.1:p.Pro339GlyfsTer12
XM_011532764.3:c.179_191dup	XP_011531066.1:p.Pro65GlyfsTer12
XM_011532765.3:c.179_191dup	XP_011531067.1:p.Pro65GlyfsTer12
XM_017003803.2:c.830_842dup	XP_016859292.1:p.Pro282GlyfsTer12
XR_001738703.2:n.1066_1078dup
NM_000821.7:c.1001_1013dup MANE Select	NP_000812.2:p.Pro339GlyfsTer12
NM_001142269.4:c.830_842dup	NP_001135741.1:p.Pro282GlyfsTer12