Canonical Allele Identifier: CA1266827798
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85558997A= , CM000664.2:g.85558997A= GRCh38
NC_000002.11:g.85786120A= , CM000664.1:g.85786120A= GRCh37
NC_000002.10:g.85639631A= NCBI36
NG_011811.2:g.7538T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.79T=
ENST00000482662.2:n.360T=
ENST00000496962.2:c.293T= ENSP00000508856.1:p.Val98=
ENST00000685865.1:n.385T=
ENST00000687250.1:n.396T=
ENST00000687995.1:n.334T=
ENST00000688205.1:c.293T= ENSP00000509673.1:p.Val98=
ENST00000688788.1:n.385T=
ENST00000689276.1:c.293T= ENSP00000510012.1:p.Val98=
ENST00000689576.1:c.293T= ENSP00000508712.1:p.Val98=
ENST00000690108.1:c.293T= ENSP00000510617.1:p.Val98=
ENST00000690468.1:c.122T= ENSP00000509078.1:p.Val41=
ENST00000690595.1:c.214+1818T= ENSP00000508979.1:n.214+1818T=
ENST00000691348.1:c.122T= ENSP00000509369.1:p.Val41=
ENST00000691410.1:c.293T= ENSP00000508479.1:p.Val98=
ENST00000693287.1:c.-67+2389T= ENSP00000510264.1:n.-67+2389T=
ENST00000693681.1:c.122T= ENSP00000510789.1:p.Val41=
ENST00000233838.9:c.293T= MANE Select ENSP00000233838.3:p.Val98=
ENST00000233838.8:c.293T= ENSP00000233838.3:p.Val98=
ENST00000421496.5:c.122T= ENSP00000400384.1:p.Val41=
ENST00000423570.5:c.293T= ENSP00000389426.1:p.Val98=
ENST00000428479.3:c.122T= ENSP00000390748.3:p.Val41=
ENST00000430215.7:c.122T= ENSP00000408045.3:p.Val41=
ENST00000465637.5:n.178+9T=
ENST00000481541.1:n.187T=
ENST00000496962.1:n.412T=
NM_000821.5:c.293T= NP_000812.2:p.Val98=
NM_000821.6:c.293T= NP_000812.2:p.Val98=
NM_001142269.2:c.122T= NP_001135741.1:p.Val41=
NM_001142269.3:c.122T= NP_001135741.1:p.Val41=
NM_001311312.1:c.293T= NP_001298241.1:p.Val98=
XM_005264259.3:c.293T= XP_005264316.1:p.Val98=
XM_011532764.1:c.-366T= XP_011531066.1:n.-366T=
XM_011532765.1:c.-366T= XP_011531067.1:n.-366T=
XR_939677.1:n.358T=
XM_005264259.5:c.293T= XP_005264316.1:p.Val98=
XM_011532764.3:c.-366T= XP_011531066.1:n.-366T=
XM_011532765.3:c.-366T= XP_011531067.1:n.-366T=
XM_017003803.2:c.122T= XP_016859292.1:p.Val41=
XR_001738703.2:n.358T=
NM_000821.7:c.293T= MANE Select NP_000812.2:p.Val98=
NM_001142269.4:c.122T= NP_001135741.1:p.Val41=
NM_001311312.2:c.293T= NP_001298241.1:p.Val98=