Canonical Allele Identifier: CA347484983
Gene: GGCX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85551932G>T , CM000664.2:g.85551932G>T GRCh38
NC_000002.11:g.85779055G>T , CM000664.1:g.85779055G>T GRCh37
NC_000002.10:g.85632566G>T NCBI36
NG_011811.2:g.14603C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.5967C>A
ENST00000482662.2:n.4374C>A
ENST00000685865.1:n.2326C>A
ENST00000687250.1:n.2026C>A
ENST00000687995.1:n.1841C>A
ENST00000688205.1:c.*1082C>A ENSP00000509673.1:n.*1082C>A
ENST00000688788.1:n.1728C>A
ENST00000689276.1:c.1420C>A ENSP00000510012.1:p.Gln474Lys
ENST00000689576.1:c.*108C>A ENSP00000508712.1:n.*108C>A
ENST00000690108.1:c.*1145C>A ENSP00000510617.1:n.*1145C>A
ENST00000690468.1:c.*41C>A ENSP00000509078.1:n.*41C>A
ENST00000690595.1:c.814C>A ENSP00000508979.1:p.Gln272Lys
ENST00000691348.1:c.*41C>A ENSP00000509369.1:n.*41C>A
ENST00000691410.1:c.*1066C>A ENSP00000508479.1:n.*1066C>A
ENST00000693287.1:c.805C>A ENSP00000510264.1:p.Gln269Lys
ENST00000693681.1:c.802C>A ENSP00000510789.1:p.Gln268Lys
ENST00000233838.9:c.1489C>A MANE Select ENSP00000233838.3:p.Gln497Lys
ENST00000233838.8:c.1489C>A ENSP00000233838.3:p.Gln497Lys
ENST00000430215.7:c.1318C>A ENSP00000408045.3:p.Gln440Lys
ENST00000465637.5:n.179-3928C>A
NM_000821.5:c.1489C>A NP_000812.2:p.Gln497Lys
NM_000821.6:c.1489C>A NP_000812.2:p.Gln497Lys
NM_001142269.2:c.1318C>A NP_001135741.1:p.Gln440Lys
NM_001142269.3:c.1318C>A NP_001135741.1:p.Gln440Lys
XM_005264259.3:c.1489C>A XP_005264316.1:p.Gln497Lys
XM_011532764.1:c.667C>A XP_011531066.1:p.Gln223Lys
XM_011532765.1:c.667C>A XP_011531067.1:p.Gln223Lys
XR_939677.1:n.1402C>A
XM_005264259.5:c.1489C>A XP_005264316.1:p.Gln497Lys
XM_011532764.3:c.667C>A XP_011531066.1:p.Gln223Lys
XM_011532765.3:c.667C>A XP_011531067.1:p.Gln223Lys
XM_017003803.2:c.1318C>A XP_016859292.1:p.Gln440Lys
XR_001738703.2:n.1402C>A
NM_000821.7:c.1489C>A MANE Select NP_000812.2:p.Gln497Lys
NM_001142269.4:c.1318C>A NP_001135741.1:p.Gln440Lys