Canonical Allele Identifier: CA1741738

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551070C>T , CM000664.2:g.85551070C>T	GRCh38
NC_000002.11:g.85778193C>T , CM000664.1:g.85778193C>T	GRCh37
NC_000002.10:g.85631704C>T	NCBI36
NG_011811.2:g.15465G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000821.7:c.1743G>A MANE Select	NP_000812.2:p.Leu581=
ENST00000233838.9:c.1743G>A MANE Select	ENSP00000233838.3:p.Leu581=
NM_000821.5:c.1743G>A	NP_000812.2:p.Leu581=
NM_000821.6:c.1743G>A	NP_000812.2:p.Leu581=
NM_001142269.2:c.1572G>A	NP_001135741.1:p.Leu524=
NM_001142269.3:c.1572G>A	NP_001135741.1:p.Leu524=
NM_001142269.4:c.1572G>A	NP_001135741.1:p.Leu524=
ENST00000233838.8:c.1743G>A	ENSP00000233838.3:p.Leu581=
ENST00000430215.7:c.1572G>A	ENSP00000408045.3:p.Leu524=
ENST00000465637.5:n.179-3066G>A
ENST00000473665.2:n.6221G>A
ENST00000482662.2:n.4628G>A
ENST00000685865.1:n.2781G>A
ENST00000687250.1:n.2280G>A
ENST00000687995.1:n.2095G>A
ENST00000688205.1:c.*1336G>A	ENSP00000509673.1:n.*1336G>A
ENST00000688788.1:n.1982G>A
ENST00000689276.1:c.1674G>A	ENSP00000510012.1:p.Leu558=
ENST00000689576.1:c.*362G>A	ENSP00000508712.1:n.*362G>A
ENST00000690108.1:c.*1399G>A	ENSP00000510617.1:n.*1399G>A
ENST00000690468.1:c.*295G>A	ENSP00000509078.1:n.*295G>A
ENST00000690595.1:c.1068G>A	ENSP00000508979.1:p.Leu356=
ENST00000691348.1:c.*295G>A	ENSP00000509369.1:n.*295G>A
ENST00000691410.1:c.*1320G>A	ENSP00000508479.1:n.*1320G>A
ENST00000693287.1:c.1059G>A	ENSP00000510264.1:p.Leu353=
ENST00000693354.1:n.253G>A
ENST00000693681.1:c.1056G>A	ENSP00000510789.1:p.Leu352=
XM_005264259.3:c.1743G>A	XP_005264316.1:p.Leu581=
XM_005264259.5:c.1743G>A	XP_005264316.1:p.Leu581=
XM_011532764.1:c.921G>A	XP_011531066.1:p.Leu307=
XM_011532764.3:c.921G>A	XP_011531066.1:p.Leu307=
XM_011532765.1:c.921G>A	XP_011531067.1:p.Leu307=
XM_011532765.3:c.921G>A	XP_011531067.1:p.Leu307=
XM_017003803.2:c.1572G>A	XP_016859292.1:p.Leu524=
XR_001738703.2:n.1656G>A
XR_939677.1:n.1656G>A