Canonical Allele Identifier: CA2659852788
Gene: GGCX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85551849_85551850insGA , CM000664.2:g.85551849_85551850insGA GRCh38
NC_000002.11:g.85778972_85778973insGA , CM000664.1:g.85778972_85778973insGA GRCh37
NC_000002.10:g.85632483_85632484insGA NCBI36
NG_011811.2:g.14685_14686insTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.6049_6050insTC
ENST00000482662.2:n.4456_4457insTC
ENST00000685865.1:n.2408_2409insTC
ENST00000687250.1:n.2108_2109insTC
ENST00000687995.1:n.1923_1924insTC
ENST00000688205.1:c.*1164_*1165insTC ENSP00000509673.1:n.*1164_*1165insTC
ENST00000688788.1:n.1810_1811insTC
ENST00000689276.1:c.1502_1503insTC ENSP00000510012.1:p.Asn502ProfsTer21
ENST00000689576.1:c.*190_*191insTC ENSP00000508712.1:n.*190_*191insTC
ENST00000690108.1:c.*1227_*1228insTC ENSP00000510617.1:n.*1227_*1228insTC
ENST00000690468.1:c.*123_*124insTC ENSP00000509078.1:n.*123_*124insTC
ENST00000690595.1:c.896_897insTC ENSP00000508979.1:p.Asn300ProfsTer21
ENST00000691348.1:c.*123_*124insTC ENSP00000509369.1:n.*123_*124insTC
ENST00000691410.1:c.*1148_*1149insTC ENSP00000508479.1:n.*1148_*1149insTC
ENST00000693287.1:c.887_888insTC ENSP00000510264.1:p.Asn297ProfsTer21
ENST00000693681.1:c.884_885insTC ENSP00000510789.1:p.Asn296ProfsTer21
ENST00000233838.9:c.1571_1572insTC MANE Select ENSP00000233838.3:p.Asn525ProfsTer21
ENST00000233838.8:c.1571_1572insTC ENSP00000233838.3:p.Asn525ProfsTer21
ENST00000430215.7:c.1400_1401insTC ENSP00000408045.3:p.Asn468ProfsTer21
ENST00000465637.5:n.179-3846_179-3845insTC
NM_000821.5:c.1571_1572insTC NP_000812.2:p.Asn525ProfsTer21
NM_000821.6:c.1571_1572insTC NP_000812.2:p.Asn525ProfsTer21
NM_001142269.2:c.1400_1401insTC NP_001135741.1:p.Asn468ProfsTer21
NM_001142269.3:c.1400_1401insTC NP_001135741.1:p.Asn468ProfsTer21
XM_005264259.3:c.1571_1572insTC XP_005264316.1:p.Asn525ProfsTer21
XM_011532764.1:c.749_750insTC XP_011531066.1:p.Asn251ProfsTer21
XM_011532765.1:c.749_750insTC XP_011531067.1:p.Asn251ProfsTer21
XR_939677.1:n.1484_1485insTC
XM_005264259.5:c.1571_1572insTC XP_005264316.1:p.Asn525ProfsTer21
XM_011532764.3:c.749_750insTC XP_011531066.1:p.Asn251ProfsTer21
XM_011532765.3:c.749_750insTC XP_011531067.1:p.Asn251ProfsTer21
XM_017003803.2:c.1400_1401insTC XP_016859292.1:p.Asn468ProfsTer21
XR_001738703.2:n.1484_1485insTC
NM_000821.7:c.1571_1572insTC MANE Select NP_000812.2:p.Asn525ProfsTer21
NM_001142269.4:c.1400_1401insTC NP_001135741.1:p.Asn468ProfsTer21