Canonical Allele Identifier: CA427440171

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85779101A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551978A>T , CM000664.2:g.85551978A>T	GRCh38
NC_000002.11:g.85779101A>T , CM000664.1:g.85779101A>T	GRCh37
NC_000002.10:g.85632612A>T	NCBI36
NG_011811.2:g.14557T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5921T>A
ENST00000482662.2:n.4328T>A
ENST00000685865.1:n.2280T>A
ENST00000687250.1:n.1980T>A
ENST00000687995.1:n.1795T>A
ENST00000688205.1:c.*1036T>A	ENSP00000509673.1:n.*1036T>A
ENST00000688788.1:n.1682T>A
ENST00000689276.1:c.1374T>A	ENSP00000510012.1:p.Ile458=
ENST00000689576.1:c.*62T>A	ENSP00000508712.1:n.*62T>A
ENST00000690108.1:c.*1099T>A	ENSP00000510617.1:n.*1099T>A
ENST00000690468.1:c.1012T>A	ENSP00000509078.1:p.Phe338Ile
ENST00000690595.1:c.768T>A	ENSP00000508979.1:p.Ile256=
ENST00000691348.1:c.1120T>A	ENSP00000509369.1:p.Phe374Ile
ENST00000691410.1:c.*1020T>A	ENSP00000508479.1:n.*1020T>A
ENST00000693287.1:c.759T>A	ENSP00000510264.1:p.Ile253=
ENST00000693681.1:c.756T>A	ENSP00000510789.1:p.Ile252=
ENST00000233838.9:c.1443T>A MANE Select	ENSP00000233838.3:p.Ile481=
ENST00000233838.8:c.1443T>A	ENSP00000233838.3:p.Ile481=
ENST00000430215.7:c.1272T>A	ENSP00000408045.3:p.Ile424=
ENST00000465637.5:n.179-3974T>A
NM_000821.5:c.1443T>A	NP_000812.2:p.Ile481=
NM_000821.6:c.1443T>A	NP_000812.2:p.Ile481=
NM_001142269.2:c.1272T>A	NP_001135741.1:p.Ile424=
NM_001142269.3:c.1272T>A	NP_001135741.1:p.Ile424=
XM_005264259.3:c.1443T>A	XP_005264316.1:p.Ile481=
XM_011532764.1:c.621T>A	XP_011531066.1:p.Ile207=
XM_011532765.1:c.621T>A	XP_011531067.1:p.Ile207=
XR_939677.1:n.1356T>A
XM_005264259.5:c.1443T>A	XP_005264316.1:p.Ile481=
XM_011532764.3:c.621T>A	XP_011531066.1:p.Ile207=
XM_011532765.3:c.621T>A	XP_011531067.1:p.Ile207=
XM_017003803.2:c.1272T>A	XP_016859292.1:p.Ile424=
XR_001738703.2:n.1356T>A
NM_000821.7:c.1443T>A MANE Select	NP_000812.2:p.Ile481=
NM_001142269.4:c.1272T>A	NP_001135741.1:p.Ile424=