Canonical Allele Identifier: CA347492177
Gene: GGCX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85558980G>T , CM000664.2:g.85558980G>T GRCh38
NC_000002.11:g.85786103G>T , CM000664.1:g.85786103G>T GRCh37
NC_000002.10:g.85639614G>T NCBI36
NG_011811.2:g.7555C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000473665.2:n.96C>A
ENST00000482662.2:n.377C>A
ENST00000496962.2:c.310C>A ENSP00000508856.1:p.Leu104Met
ENST00000685865.1:n.402C>A
ENST00000687250.1:n.413C>A
ENST00000687995.1:n.351C>A
ENST00000688205.1:c.310C>A ENSP00000509673.1:p.Leu104Met
ENST00000688788.1:n.402C>A
ENST00000689276.1:c.310C>A ENSP00000510012.1:p.Leu104Met
ENST00000689576.1:c.310C>A ENSP00000508712.1:p.Leu104Met
ENST00000690108.1:c.310C>A ENSP00000510617.1:p.Leu104Met
ENST00000690468.1:c.139C>A ENSP00000509078.1:p.Leu47Met
ENST00000690595.1:c.214+1835C>A ENSP00000508979.1:n.214+1835C>A
ENST00000691348.1:c.139C>A ENSP00000509369.1:p.Leu47Met
ENST00000691410.1:c.310C>A ENSP00000508479.1:p.Leu104Met
ENST00000693287.1:c.-67+2406C>A ENSP00000510264.1:n.-67+2406C>A
ENST00000693681.1:c.139C>A ENSP00000510789.1:p.Leu47Met
ENST00000233838.9:c.310C>A MANE Select ENSP00000233838.3:p.Leu104Met
ENST00000233838.8:c.310C>A ENSP00000233838.3:p.Leu104Met
ENST00000421496.5:c.139C>A ENSP00000400384.1:p.Leu47Met
ENST00000423570.5:c.310C>A ENSP00000389426.1:p.Leu104Met
ENST00000428479.3:c.139C>A ENSP00000390748.3:p.Leu47Met
ENST00000430215.7:c.139C>A ENSP00000408045.3:p.Leu47Met
ENST00000465637.5:n.178+26C>A
ENST00000481541.1:n.204C>A
ENST00000496962.1:n.429C>A
NM_000821.5:c.310C>A NP_000812.2:p.Leu104Met
NM_000821.6:c.310C>A NP_000812.2:p.Leu104Met
NM_001142269.2:c.139C>A NP_001135741.1:p.Leu47Met
NM_001142269.3:c.139C>A NP_001135741.1:p.Leu47Met
NM_001311312.1:c.310C>A NP_001298241.1:p.Leu104Met
XM_005264259.3:c.310C>A XP_005264316.1:p.Leu104Met
XM_011532764.1:c.-349C>A XP_011531066.1:n.-349C>A
XM_011532765.1:c.-349C>A XP_011531067.1:n.-349C>A
XR_939677.1:n.375C>A
XM_005264259.5:c.310C>A XP_005264316.1:p.Leu104Met
XM_011532764.3:c.-349C>A XP_011531066.1:n.-349C>A
XM_011532765.3:c.-349C>A XP_011531067.1:n.-349C>A
XM_017003803.2:c.139C>A XP_016859292.1:p.Leu47Met
XR_001738703.2:n.375C>A
NM_000821.7:c.310C>A MANE Select NP_000812.2:p.Leu104Met
NM_001142269.4:c.139C>A NP_001135741.1:p.Leu47Met
NM_001311312.2:c.310C>A NP_001298241.1:p.Leu104Met