Canonical Allele Identifier: CA347492119

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85786082G>C (hg19) ; chr2:g.85558959G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85558959G>C , CM000664.2:g.85558959G>C	GRCh38
NC_000002.11:g.85786082G>C , CM000664.1:g.85786082G>C	GRCh37
NC_000002.10:g.85639593G>C	NCBI36
NG_011811.2:g.7576C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.117C>G
ENST00000482662.2:n.398C>G
ENST00000496962.2:c.331C>G	ENSP00000508856.1:p.Pro111Ala
ENST00000685865.1:n.423C>G
ENST00000687250.1:n.434C>G
ENST00000687995.1:n.372C>G
ENST00000688205.1:c.331C>G	ENSP00000509673.1:p.Pro111Ala
ENST00000688788.1:n.423C>G
ENST00000689276.1:c.331C>G	ENSP00000510012.1:p.Pro111Ala
ENST00000689576.1:c.331C>G	ENSP00000508712.1:p.Pro111Ala
ENST00000690108.1:c.331C>G	ENSP00000510617.1:p.Pro111Ala
ENST00000690468.1:c.160C>G	ENSP00000509078.1:p.Pro54Ala
ENST00000690595.1:c.214+1856C>G	ENSP00000508979.1:n.214+1856C>G
ENST00000691348.1:c.160C>G	ENSP00000509369.1:p.Pro54Ala
ENST00000691410.1:c.331C>G	ENSP00000508479.1:p.Pro111Ala
ENST00000693287.1:c.-67+2427C>G	ENSP00000510264.1:n.-67+2427C>G
ENST00000693681.1:c.160C>G	ENSP00000510789.1:p.Pro54Ala
ENST00000233838.9:c.331C>G MANE Select	ENSP00000233838.3:p.Pro111Ala
ENST00000233838.8:c.331C>G	ENSP00000233838.3:p.Pro111Ala
ENST00000421496.5:c.160C>G	ENSP00000400384.1:p.Pro54Ala
ENST00000423570.5:c.331C>G	ENSP00000389426.1:p.Pro111Ala
ENST00000428479.3:c.160C>G	ENSP00000390748.3:p.Pro54Ala
ENST00000430215.7:c.160C>G	ENSP00000408045.3:p.Pro54Ala
ENST00000465637.5:n.178+47C>G
ENST00000481541.1:n.225C>G
ENST00000496962.1:n.450C>G
NM_000821.5:c.331C>G	NP_000812.2:p.Pro111Ala
NM_000821.6:c.331C>G	NP_000812.2:p.Pro111Ala
NM_001142269.2:c.160C>G	NP_001135741.1:p.Pro54Ala
NM_001142269.3:c.160C>G	NP_001135741.1:p.Pro54Ala
NM_001311312.1:c.331C>G	NP_001298241.1:p.Pro111Ala
XM_005264259.3:c.331C>G	XP_005264316.1:p.Pro111Ala
XM_011532764.1:c.-328C>G	XP_011531066.1:n.-328C>G
XM_011532765.1:c.-328C>G	XP_011531067.1:n.-328C>G
XR_939677.1:n.396C>G
XM_005264259.5:c.331C>G	XP_005264316.1:p.Pro111Ala
XM_011532764.3:c.-328C>G	XP_011531066.1:n.-328C>G
XM_011532765.3:c.-328C>G	XP_011531067.1:n.-328C>G
XM_017003803.2:c.160C>G	XP_016859292.1:p.Pro54Ala
XR_001738703.2:n.396C>G
NM_000821.7:c.331C>G MANE Select	NP_000812.2:p.Pro111Ala
NM_001142269.4:c.160C>G	NP_001135741.1:p.Pro54Ala
NM_001311312.2:c.331C>G	NP_001298241.1:p.Pro111Ala