Canonical Allele Identifier: CA347484785
Gene: GGCX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85551843G>T , CM000664.2:g.85551843G>T GRCh38
NC_000002.11:g.85778966G>T , CM000664.1:g.85778966G>T GRCh37
NC_000002.10:g.85632477G>T NCBI36
NG_011811.2:g.14692C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.6056C>A
ENST00000482662.2:n.4463C>A
ENST00000685865.1:n.2415C>A
ENST00000687250.1:n.2115C>A
ENST00000687995.1:n.1930C>A
ENST00000688205.1:c.*1171C>A ENSP00000509673.1:n.*1171C>A
ENST00000688788.1:n.1817C>A
ENST00000689276.1:c.1509C>A ENSP00000510012.1:p.His503Gln
ENST00000689576.1:c.*197C>A ENSP00000508712.1:n.*197C>A
ENST00000690108.1:c.*1234C>A ENSP00000510617.1:n.*1234C>A
ENST00000690468.1:c.*130C>A ENSP00000509078.1:n.*130C>A
ENST00000690595.1:c.903C>A ENSP00000508979.1:p.His301Gln
ENST00000691348.1:c.*130C>A ENSP00000509369.1:n.*130C>A
ENST00000691410.1:c.*1155C>A ENSP00000508479.1:n.*1155C>A
ENST00000693287.1:c.894C>A ENSP00000510264.1:p.His298Gln
ENST00000693681.1:c.891C>A ENSP00000510789.1:p.His297Gln
ENST00000233838.9:c.1578C>A MANE Select ENSP00000233838.3:p.His526Gln
ENST00000233838.8:c.1578C>A ENSP00000233838.3:p.His526Gln
ENST00000430215.7:c.1407C>A ENSP00000408045.3:p.His469Gln
ENST00000465637.5:n.179-3839C>A
NM_000821.5:c.1578C>A NP_000812.2:p.His526Gln
NM_000821.6:c.1578C>A NP_000812.2:p.His526Gln
NM_001142269.2:c.1407C>A NP_001135741.1:p.His469Gln
NM_001142269.3:c.1407C>A NP_001135741.1:p.His469Gln
XM_005264259.3:c.1578C>A XP_005264316.1:p.His526Gln
XM_011532764.1:c.756C>A XP_011531066.1:p.His252Gln
XM_011532765.1:c.756C>A XP_011531067.1:p.His252Gln
XR_939677.1:n.1491C>A
XM_005264259.5:c.1578C>A XP_005264316.1:p.His526Gln
XM_011532764.3:c.756C>A XP_011531066.1:p.His252Gln
XM_011532765.3:c.756C>A XP_011531067.1:p.His252Gln
XM_017003803.2:c.1407C>A XP_016859292.1:p.His469Gln
XR_001738703.2:n.1491C>A
NM_000821.7:c.1578C>A MANE Select NP_000812.2:p.His526Gln
NM_001142269.4:c.1407C>A NP_001135741.1:p.His469Gln