Canonical Allele Identifier: CA347487012

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85780143C>G (hg19) ; chr2:g.85553020C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553020C>G , CM000664.2:g.85553020C>G	GRCh38
NC_000002.11:g.85780143C>G , CM000664.1:g.85780143C>G	GRCh37
NC_000002.10:g.85633654C>G	NCBI36
NG_011811.2:g.13515G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5250G>C
ENST00000482662.2:n.3657G>C
ENST00000685865.1:n.1609G>C
ENST00000687250.1:n.1309G>C
ENST00000687995.1:n.1558G>C
ENST00000688205.1:c.*799G>C	ENSP00000509673.1:n.*799G>C
ENST00000688788.1:n.1445G>C
ENST00000689276.1:c.1137G>C	ENSP00000510012.1:p.Met379Ile
ENST00000689576.1:c.1206G>C	ENSP00000508712.1:p.Met402Ile
ENST00000690108.1:c.*862G>C	ENSP00000510617.1:n.*862G>C
ENST00000690468.1:c.927G>C	ENSP00000509078.1:p.Met309Ile
ENST00000690595.1:c.531G>C	ENSP00000508979.1:p.Met177Ile
ENST00000691348.1:c.1035G>C	ENSP00000509369.1:p.Met345Ile
ENST00000691410.1:c.*783G>C	ENSP00000508479.1:n.*783G>C
ENST00000693287.1:c.522G>C	ENSP00000510264.1:p.Met174Ile
ENST00000693681.1:c.519G>C	ENSP00000510789.1:p.Met173Ile
ENST00000233838.9:c.1206G>C MANE Select	ENSP00000233838.3:p.Met402Ile
ENST00000233838.8:c.1206G>C	ENSP00000233838.3:p.Met402Ile
ENST00000430215.7:c.1035G>C	ENSP00000408045.3:p.Met345Ile
ENST00000465637.5:n.179-5016G>C
ENST00000473665.1:n.699G>C
ENST00000482662.1:n.623G>C
NM_000821.5:c.1206G>C	NP_000812.2:p.Met402Ile
NM_000821.6:c.1206G>C	NP_000812.2:p.Met402Ile
NM_001142269.2:c.1035G>C	NP_001135741.1:p.Met345Ile
NM_001142269.3:c.1035G>C	NP_001135741.1:p.Met345Ile
XM_005264259.3:c.1206G>C	XP_005264316.1:p.Met402Ile
XM_011532764.1:c.384G>C	XP_011531066.1:p.Met128Ile
XM_011532765.1:c.384G>C	XP_011531067.1:p.Met128Ile
XR_939677.1:n.1271G>C
XM_005264259.5:c.1206G>C	XP_005264316.1:p.Met402Ile
XM_011532764.3:c.384G>C	XP_011531066.1:p.Met128Ile
XM_011532765.3:c.384G>C	XP_011531067.1:p.Met128Ile
XM_017003803.2:c.1035G>C	XP_016859292.1:p.Met345Ile
XR_001738703.2:n.1271G>C
NM_000821.7:c.1206G>C MANE Select	NP_000812.2:p.Met402Ile
NM_001142269.4:c.1035G>C	NP_001135741.1:p.Met345Ile