Canonical Allele Identifier: CA427440174

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85779104C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551981C>T , CM000664.2:g.85551981C>T	GRCh38
NC_000002.11:g.85779104C>T , CM000664.1:g.85779104C>T	GRCh37
NC_000002.10:g.85632615C>T	NCBI36
NG_011811.2:g.14554G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5918G>A
ENST00000482662.2:n.4325G>A
ENST00000685865.1:n.2277G>A
ENST00000687250.1:n.1977G>A
ENST00000687995.1:n.1792G>A
ENST00000688205.1:c.*1033G>A	ENSP00000509673.1:n.*1033G>A
ENST00000688788.1:n.1679G>A
ENST00000689276.1:c.1371G>A	ENSP00000510012.1:p.Arg457=
ENST00000689576.1:c.*59G>A	ENSP00000508712.1:n.*59G>A
ENST00000690108.1:c.*1096G>A	ENSP00000510617.1:n.*1096G>A
ENST00000690468.1:c.1009G>A	ENSP00000509078.1:p.Asp337Asn
ENST00000690595.1:c.765G>A	ENSP00000508979.1:p.Arg255=
ENST00000691348.1:c.1117G>A	ENSP00000509369.1:p.Asp373Asn
ENST00000691410.1:c.*1017G>A	ENSP00000508479.1:n.*1017G>A
ENST00000693287.1:c.756G>A	ENSP00000510264.1:p.Arg252=
ENST00000693681.1:c.753G>A	ENSP00000510789.1:p.Arg251=
ENST00000233838.9:c.1440G>A MANE Select	ENSP00000233838.3:p.Arg480=
ENST00000233838.8:c.1440G>A	ENSP00000233838.3:p.Arg480=
ENST00000430215.7:c.1269G>A	ENSP00000408045.3:p.Arg423=
ENST00000465637.5:n.179-3977G>A
NM_000821.5:c.1440G>A	NP_000812.2:p.Arg480=
NM_000821.6:c.1440G>A	NP_000812.2:p.Arg480=
NM_001142269.2:c.1269G>A	NP_001135741.1:p.Arg423=
NM_001142269.3:c.1269G>A	NP_001135741.1:p.Arg423=
XM_005264259.3:c.1440G>A	XP_005264316.1:p.Arg480=
XM_011532764.1:c.618G>A	XP_011531066.1:p.Arg206=
XM_011532765.1:c.618G>A	XP_011531067.1:p.Arg206=
XR_939677.1:n.1353G>A
XM_005264259.5:c.1440G>A	XP_005264316.1:p.Arg480=
XM_011532764.3:c.618G>A	XP_011531066.1:p.Arg206=
XM_011532765.3:c.618G>A	XP_011531067.1:p.Arg206=
XM_017003803.2:c.1269G>A	XP_016859292.1:p.Arg423=
XR_001738703.2:n.1353G>A
NM_000821.7:c.1440G>A MANE Select	NP_000812.2:p.Arg480=
NM_001142269.4:c.1269G>A	NP_001135741.1:p.Arg423=