Canonical Allele Identifier: CA427440033

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85778972G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551849G>A , CM000664.2:g.85551849G>A	GRCh38
NC_000002.11:g.85778972G>A , CM000664.1:g.85778972G>A	GRCh37
NC_000002.10:g.85632483G>A	NCBI36
NG_011811.2:g.14686C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.6050C>T
ENST00000482662.2:n.4457C>T
ENST00000685865.1:n.2409C>T
ENST00000687250.1:n.2109C>T
ENST00000687995.1:n.1924C>T
ENST00000688205.1:c.*1165C>T	ENSP00000509673.1:n.*1165C>T
ENST00000688788.1:n.1811C>T
ENST00000689276.1:c.1503C>T	ENSP00000510012.1:p.Asp501=
ENST00000689576.1:c.*191C>T	ENSP00000508712.1:n.*191C>T
ENST00000690108.1:c.*1228C>T	ENSP00000510617.1:n.*1228C>T
ENST00000690468.1:c.*124C>T	ENSP00000509078.1:n.*124C>T
ENST00000690595.1:c.897C>T	ENSP00000508979.1:p.Asp299=
ENST00000691348.1:c.*124C>T	ENSP00000509369.1:n.*124C>T
ENST00000691410.1:c.*1149C>T	ENSP00000508479.1:n.*1149C>T
ENST00000693287.1:c.888C>T	ENSP00000510264.1:p.Asp296=
ENST00000693681.1:c.885C>T	ENSP00000510789.1:p.Asp295=
ENST00000233838.9:c.1572C>T MANE Select	ENSP00000233838.3:p.Asp524=
ENST00000233838.8:c.1572C>T	ENSP00000233838.3:p.Asp524=
ENST00000430215.7:c.1401C>T	ENSP00000408045.3:p.Asp467=
ENST00000465637.5:n.179-3845C>T
NM_000821.5:c.1572C>T	NP_000812.2:p.Asp524=
NM_000821.6:c.1572C>T	NP_000812.2:p.Asp524=
NM_001142269.2:c.1401C>T	NP_001135741.1:p.Asp467=
NM_001142269.3:c.1401C>T	NP_001135741.1:p.Asp467=
XM_005264259.3:c.1572C>T	XP_005264316.1:p.Asp524=
XM_011532764.1:c.750C>T	XP_011531066.1:p.Asp250=
XM_011532765.1:c.750C>T	XP_011531067.1:p.Asp250=
XR_939677.1:n.1485C>T
XM_005264259.5:c.1572C>T	XP_005264316.1:p.Asp524=
XM_011532764.3:c.750C>T	XP_011531066.1:p.Asp250=
XM_011532765.3:c.750C>T	XP_011531067.1:p.Asp250=
XM_017003803.2:c.1401C>T	XP_016859292.1:p.Asp467=
XR_001738703.2:n.1485C>T
NM_000821.7:c.1572C>T MANE Select	NP_000812.2:p.Asp524=
NM_001142269.4:c.1401C>T	NP_001135741.1:p.Asp467=