Canonical Allele Identifier: CA1266827805
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85559014G= , CM000664.2:g.85559014G= GRCh38
NC_000002.11:g.85786137G= , CM000664.1:g.85786137G= GRCh37
NC_000002.10:g.85639648G= NCBI36
NG_011811.2:g.7521C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.62C=
ENST00000482662.2:n.343C=
ENST00000496962.2:c.276C= ENSP00000508856.1:p.Tyr92=
ENST00000685865.1:n.368C=
ENST00000687250.1:n.379C=
ENST00000687995.1:n.317C=
ENST00000688205.1:c.276C= ENSP00000509673.1:p.Tyr92=
ENST00000688788.1:n.368C=
ENST00000689276.1:c.276C= ENSP00000510012.1:p.Tyr92=
ENST00000689576.1:c.276C= ENSP00000508712.1:p.Tyr92=
ENST00000690108.1:c.276C= ENSP00000510617.1:p.Tyr92=
ENST00000690468.1:c.105C= ENSP00000509078.1:p.Tyr35=
ENST00000690595.1:c.214+1801C= ENSP00000508979.1:n.214+1801C=
ENST00000691348.1:c.105C= ENSP00000509369.1:p.Tyr35=
ENST00000691410.1:c.276C= ENSP00000508479.1:p.Tyr92=
ENST00000693287.1:c.-67+2372C= ENSP00000510264.1:n.-67+2372C=
ENST00000693681.1:c.105C= ENSP00000510789.1:p.Tyr35=
ENST00000233838.9:c.276C= MANE Select ENSP00000233838.3:p.Tyr92=
ENST00000233838.8:c.276C= ENSP00000233838.3:p.Tyr92=
ENST00000421496.5:c.105C= ENSP00000400384.1:p.Tyr35=
ENST00000423570.5:c.276C= ENSP00000389426.1:p.Tyr92=
ENST00000428479.3:c.105C= ENSP00000390748.3:p.Tyr35=
ENST00000430215.7:c.105C= ENSP00000408045.3:p.Tyr35=
ENST00000465637.5:n.170C=
ENST00000481541.1:n.170C=
ENST00000496962.1:n.395C=
NM_000821.5:c.276C= NP_000812.2:p.Tyr92=
NM_000821.6:c.276C= NP_000812.2:p.Tyr92=
NM_001142269.2:c.105C= NP_001135741.1:p.Tyr35=
NM_001142269.3:c.105C= NP_001135741.1:p.Tyr35=
NM_001311312.1:c.276C= NP_001298241.1:p.Tyr92=
XM_005264259.3:c.276C= XP_005264316.1:p.Tyr92=
XM_011532764.1:c.-383C= XP_011531066.1:n.-383C=
XM_011532765.1:c.-383C= XP_011531067.1:n.-383C=
XR_939677.1:n.341C=
XM_005264259.5:c.276C= XP_005264316.1:p.Tyr92=
XM_011532764.3:c.-383C= XP_011531066.1:n.-383C=
XM_011532765.3:c.-383C= XP_011531067.1:n.-383C=
XM_017003803.2:c.105C= XP_016859292.1:p.Tyr35=
XR_001738703.2:n.341C=
NM_000821.7:c.276C= MANE Select NP_000812.2:p.Tyr92=
NM_001142269.4:c.105C= NP_001135741.1:p.Tyr35=
NM_001311312.2:c.276C= NP_001298241.1:p.Tyr92=