Canonical Allele Identifier: CA427440044

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85778987G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551864G>A , CM000664.2:g.85551864G>A	GRCh38
NC_000002.11:g.85778987G>A , CM000664.1:g.85778987G>A	GRCh37
NC_000002.10:g.85632498G>A	NCBI36
NG_011811.2:g.14671C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.6035C>T
ENST00000482662.2:n.4442C>T
ENST00000685865.1:n.2394C>T
ENST00000687250.1:n.2094C>T
ENST00000687995.1:n.1909C>T
ENST00000688205.1:c.*1150C>T	ENSP00000509673.1:n.*1150C>T
ENST00000688788.1:n.1796C>T
ENST00000689276.1:c.1488C>T	ENSP00000510012.1:p.Ile496=
ENST00000689576.1:c.*176C>T	ENSP00000508712.1:n.*176C>T
ENST00000690108.1:c.*1213C>T	ENSP00000510617.1:n.*1213C>T
ENST00000690468.1:c.*109C>T	ENSP00000509078.1:n.*109C>T
ENST00000690595.1:c.882C>T	ENSP00000508979.1:p.Ile294=
ENST00000691348.1:c.*109C>T	ENSP00000509369.1:n.*109C>T
ENST00000691410.1:c.*1134C>T	ENSP00000508479.1:n.*1134C>T
ENST00000693287.1:c.873C>T	ENSP00000510264.1:p.Ile291=
ENST00000693681.1:c.870C>T	ENSP00000510789.1:p.Ile290=
ENST00000233838.9:c.1557C>T MANE Select	ENSP00000233838.3:p.Ile519=
ENST00000233838.8:c.1557C>T	ENSP00000233838.3:p.Ile519=
ENST00000430215.7:c.1386C>T	ENSP00000408045.3:p.Ile462=
ENST00000465637.5:n.179-3860C>T
NM_000821.5:c.1557C>T	NP_000812.2:p.Ile519=
NM_000821.6:c.1557C>T	NP_000812.2:p.Ile519=
NM_001142269.2:c.1386C>T	NP_001135741.1:p.Ile462=
NM_001142269.3:c.1386C>T	NP_001135741.1:p.Ile462=
XM_005264259.3:c.1557C>T	XP_005264316.1:p.Ile519=
XM_011532764.1:c.735C>T	XP_011531066.1:p.Ile245=
XM_011532765.1:c.735C>T	XP_011531067.1:p.Ile245=
XR_939677.1:n.1470C>T
XM_005264259.5:c.1557C>T	XP_005264316.1:p.Ile519=
XM_011532764.3:c.735C>T	XP_011531066.1:p.Ile245=
XM_011532765.3:c.735C>T	XP_011531067.1:p.Ile245=
XM_017003803.2:c.1386C>T	XP_016859292.1:p.Ile462=
XR_001738703.2:n.1470C>T
NM_000821.7:c.1557C>T MANE Select	NP_000812.2:p.Ile519=
NM_001142269.4:c.1386C>T	NP_001135741.1:p.Ile462=