Canonical Allele Identifier: CA427440012

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85778957C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551834C>G , CM000664.2:g.85551834C>G	GRCh38
NC_000002.11:g.85778957C>G , CM000664.1:g.85778957C>G	GRCh37
NC_000002.10:g.85632468C>G	NCBI36
NG_011811.2:g.14701G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.6065G>C
ENST00000482662.2:n.4472G>C
ENST00000685865.1:n.2424G>C
ENST00000687250.1:n.2124G>C
ENST00000687995.1:n.1939G>C
ENST00000688205.1:c.*1180G>C	ENSP00000509673.1:n.*1180G>C
ENST00000688788.1:n.1826G>C
ENST00000689276.1:c.1518G>C	ENSP00000510012.1:p.Val506=
ENST00000689576.1:c.*206G>C	ENSP00000508712.1:n.*206G>C
ENST00000690108.1:c.*1243G>C	ENSP00000510617.1:n.*1243G>C
ENST00000690468.1:c.*139G>C	ENSP00000509078.1:n.*139G>C
ENST00000690595.1:c.912G>C	ENSP00000508979.1:p.Val304=
ENST00000691348.1:c.*139G>C	ENSP00000509369.1:n.*139G>C
ENST00000691410.1:c.*1164G>C	ENSP00000508479.1:n.*1164G>C
ENST00000693287.1:c.903G>C	ENSP00000510264.1:p.Val301=
ENST00000693681.1:c.900G>C	ENSP00000510789.1:p.Val300=
ENST00000233838.9:c.1587G>C MANE Select	ENSP00000233838.3:p.Val529=
ENST00000233838.8:c.1587G>C	ENSP00000233838.3:p.Val529=
ENST00000430215.7:c.1416G>C	ENSP00000408045.3:p.Val472=
ENST00000465637.5:n.179-3830G>C
NM_000821.5:c.1587G>C	NP_000812.2:p.Val529=
NM_000821.6:c.1587G>C	NP_000812.2:p.Val529=
NM_001142269.2:c.1416G>C	NP_001135741.1:p.Val472=
NM_001142269.3:c.1416G>C	NP_001135741.1:p.Val472=
XM_005264259.3:c.1587G>C	XP_005264316.1:p.Val529=
XM_011532764.1:c.765G>C	XP_011531066.1:p.Val255=
XM_011532765.1:c.765G>C	XP_011531067.1:p.Val255=
XR_939677.1:n.1500G>C
XM_005264259.5:c.1587G>C	XP_005264316.1:p.Val529=
XM_011532764.3:c.765G>C	XP_011531066.1:p.Val255=
XM_011532765.3:c.765G>C	XP_011531067.1:p.Val255=
XM_017003803.2:c.1416G>C	XP_016859292.1:p.Val472=
XR_001738703.2:n.1500G>C
NM_000821.7:c.1587G>C MANE Select	NP_000812.2:p.Val529=
NM_001142269.4:c.1416G>C	NP_001135741.1:p.Val472=