Canonical Allele Identifier: CA427091999

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85786077A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85558954A>G , CM000664.2:g.85558954A>G	GRCh38
NC_000002.11:g.85786077A>G , CM000664.1:g.85786077A>G	GRCh37
NC_000002.10:g.85639588A>G	NCBI36
NG_011811.2:g.7581T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.122T>C
ENST00000482662.2:n.403T>C
ENST00000496962.2:c.336T>C	ENSP00000508856.1:p.Leu112=
ENST00000685865.1:n.428T>C
ENST00000687250.1:n.439T>C
ENST00000687995.1:n.377T>C
ENST00000688205.1:c.336T>C	ENSP00000509673.1:p.Leu112=
ENST00000688788.1:n.428T>C
ENST00000689276.1:c.336T>C	ENSP00000510012.1:p.Leu112=
ENST00000689576.1:c.336T>C	ENSP00000508712.1:p.Leu112=
ENST00000690108.1:c.336T>C	ENSP00000510617.1:p.Leu112=
ENST00000690468.1:c.165T>C	ENSP00000509078.1:p.Leu55=
ENST00000690595.1:c.214+1861T>C	ENSP00000508979.1:n.214+1861T>C
ENST00000691348.1:c.165T>C	ENSP00000509369.1:p.Leu55=
ENST00000691410.1:c.336T>C	ENSP00000508479.1:p.Leu112=
ENST00000693287.1:c.-67+2432T>C	ENSP00000510264.1:n.-67+2432T>C
ENST00000693681.1:c.165T>C	ENSP00000510789.1:p.Leu55=
ENST00000233838.9:c.336T>C MANE Select	ENSP00000233838.3:p.Leu112=
ENST00000233838.8:c.336T>C	ENSP00000233838.3:p.Leu112=
ENST00000421496.5:c.165T>C	ENSP00000400384.1:p.Leu55=
ENST00000423570.5:c.336T>C	ENSP00000389426.1:p.Leu112=
ENST00000428479.3:c.165T>C	ENSP00000390748.3:p.Leu55=
ENST00000430215.7:c.165T>C	ENSP00000408045.3:p.Leu55=
ENST00000465637.5:n.178+52T>C
ENST00000481541.1:n.230T>C
ENST00000496962.1:n.455T>C
NM_000821.5:c.336T>C	NP_000812.2:p.Leu112=
NM_000821.6:c.336T>C	NP_000812.2:p.Leu112=
NM_001142269.2:c.165T>C	NP_001135741.1:p.Leu55=
NM_001142269.3:c.165T>C	NP_001135741.1:p.Leu55=
NM_001311312.1:c.336T>C	NP_001298241.1:p.Leu112=
XM_005264259.3:c.336T>C	XP_005264316.1:p.Leu112=
XM_011532764.1:c.-323T>C	XP_011531066.1:n.-323T>C
XM_011532765.1:c.-323T>C	XP_011531067.1:n.-323T>C
XR_939677.1:n.401T>C
XM_005264259.5:c.336T>C	XP_005264316.1:p.Leu112=
XM_011532764.3:c.-323T>C	XP_011531066.1:n.-323T>C
XM_011532765.3:c.-323T>C	XP_011531067.1:n.-323T>C
XM_017003803.2:c.165T>C	XP_016859292.1:p.Leu55=
XR_001738703.2:n.401T>C
NM_000821.7:c.336T>C MANE Select	NP_000812.2:p.Leu112=
NM_001142269.4:c.165T>C	NP_001135741.1:p.Leu55=
NM_001311312.2:c.336T>C	NP_001298241.1:p.Leu112=