Canonical Allele Identifier: CA427092469

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85786185C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85559062C>T , CM000664.2:g.85559062C>T	GRCh38
NC_000002.11:g.85786185C>T , CM000664.1:g.85786185C>T	GRCh37
NC_000002.10:g.85639696C>T	NCBI36
NG_011811.2:g.7473G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.14G>A
ENST00000482662.2:n.295G>A
ENST00000496962.2:c.228G>A	ENSP00000508856.1:p.Val76=
ENST00000685865.1:n.320G>A
ENST00000687250.1:n.331G>A
ENST00000687995.1:n.269G>A
ENST00000688205.1:c.228G>A	ENSP00000509673.1:p.Val76=
ENST00000688788.1:n.320G>A
ENST00000689276.1:c.228G>A	ENSP00000510012.1:p.Val76=
ENST00000689576.1:c.228G>A	ENSP00000508712.1:p.Val76=
ENST00000690108.1:c.228G>A	ENSP00000510617.1:p.Val76=
ENST00000690468.1:c.57G>A	ENSP00000509078.1:p.Val19=
ENST00000690595.1:c.214+1753G>A	ENSP00000508979.1:n.214+1753G>A
ENST00000691348.1:c.57G>A	ENSP00000509369.1:p.Val19=
ENST00000691410.1:c.228G>A	ENSP00000508479.1:p.Val76=
ENST00000693287.1:c.-67+2324G>A	ENSP00000510264.1:n.-67+2324G>A
ENST00000693681.1:c.57G>A	ENSP00000510789.1:p.Val19=
ENST00000233838.9:c.228G>A MANE Select	ENSP00000233838.3:p.Val76=
ENST00000233838.8:c.228G>A	ENSP00000233838.3:p.Val76=
ENST00000421496.5:c.57G>A	ENSP00000400384.1:p.Val19=
ENST00000423570.5:c.228G>A	ENSP00000389426.1:p.Val76=
ENST00000428479.3:c.57G>A	ENSP00000390748.3:p.Val19=
ENST00000430215.7:c.57G>A	ENSP00000408045.3:p.Val19=
ENST00000465637.5:n.122G>A
ENST00000481541.1:n.122G>A
ENST00000496962.1:n.347G>A
NM_000821.5:c.228G>A	NP_000812.2:p.Val76=
NM_000821.6:c.228G>A	NP_000812.2:p.Val76=
NM_001142269.2:c.57G>A	NP_001135741.1:p.Val19=
NM_001142269.3:c.57G>A	NP_001135741.1:p.Val19=
NM_001311312.1:c.228G>A	NP_001298241.1:p.Val76=
XM_005264259.3:c.228G>A	XP_005264316.1:p.Val76=
XM_011532764.1:c.-431G>A	XP_011531066.1:n.-431G>A
XM_011532765.1:c.-431G>A	XP_011531067.1:n.-431G>A
XR_939677.1:n.293G>A
XM_005264259.5:c.228G>A	XP_005264316.1:p.Val76=
XM_011532764.3:c.-431G>A	XP_011531066.1:n.-431G>A
XM_011532765.3:c.-431G>A	XP_011531067.1:n.-431G>A
XM_017003803.2:c.57G>A	XP_016859292.1:p.Val19=
XR_001738703.2:n.293G>A
NM_000821.7:c.228G>A MANE Select	NP_000812.2:p.Val76=
NM_001142269.4:c.57G>A	NP_001135741.1:p.Val19=
NM_001311312.2:c.228G>A	NP_001298241.1:p.Val76=