Canonical Allele Identifier: CA427440081

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85779011G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551888G>T , CM000664.2:g.85551888G>T	GRCh38
NC_000002.11:g.85779011G>T , CM000664.1:g.85779011G>T	GRCh37
NC_000002.10:g.85632522G>T	NCBI36
NG_011811.2:g.14647C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.6011C>A
ENST00000482662.2:n.4418C>A
ENST00000685865.1:n.2370C>A
ENST00000687250.1:n.2070C>A
ENST00000687995.1:n.1885C>A
ENST00000688205.1:c.*1126C>A	ENSP00000509673.1:n.*1126C>A
ENST00000688788.1:n.1772C>A
ENST00000689276.1:c.1464C>A	ENSP00000510012.1:p.Pro488=
ENST00000689576.1:c.*152C>A	ENSP00000508712.1:n.*152C>A
ENST00000690108.1:c.*1189C>A	ENSP00000510617.1:n.*1189C>A
ENST00000690468.1:c.*85C>A	ENSP00000509078.1:n.*85C>A
ENST00000690595.1:c.858C>A	ENSP00000508979.1:p.Pro286=
ENST00000691348.1:c.*85C>A	ENSP00000509369.1:n.*85C>A
ENST00000691410.1:c.*1110C>A	ENSP00000508479.1:n.*1110C>A
ENST00000693287.1:c.849C>A	ENSP00000510264.1:p.Pro283=
ENST00000693681.1:c.846C>A	ENSP00000510789.1:p.Pro282=
ENST00000233838.9:c.1533C>A MANE Select	ENSP00000233838.3:p.Pro511=
ENST00000233838.8:c.1533C>A	ENSP00000233838.3:p.Pro511=
ENST00000430215.7:c.1362C>A	ENSP00000408045.3:p.Pro454=
ENST00000465637.5:n.179-3884C>A
NM_000821.5:c.1533C>A	NP_000812.2:p.Pro511=
NM_000821.6:c.1533C>A	NP_000812.2:p.Pro511=
NM_001142269.2:c.1362C>A	NP_001135741.1:p.Pro454=
NM_001142269.3:c.1362C>A	NP_001135741.1:p.Pro454=
XM_005264259.3:c.1533C>A	XP_005264316.1:p.Pro511=
XM_011532764.1:c.711C>A	XP_011531066.1:p.Pro237=
XM_011532765.1:c.711C>A	XP_011531067.1:p.Pro237=
XR_939677.1:n.1446C>A
XM_005264259.5:c.1533C>A	XP_005264316.1:p.Pro511=
XM_011532764.3:c.711C>A	XP_011531066.1:p.Pro237=
XM_011532765.3:c.711C>A	XP_011531067.1:p.Pro237=
XM_017003803.2:c.1362C>A	XP_016859292.1:p.Pro454=
XR_001738703.2:n.1446C>A
NM_000821.7:c.1533C>A MANE Select	NP_000812.2:p.Pro511=
NM_001142269.4:c.1362C>A	NP_001135741.1:p.Pro454=