Canonical Allele Identifier: CA1266827773
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85558924_85558927delinsCATG , CM000664.2:g.85558924_85558927delinsCATG GRCh38
NC_000002.11:g.85786047_85786050delinsCATG , CM000664.1:g.85786047_85786050delinsCATG GRCh37
NC_000002.10:g.85639558_85639561delinsCATG NCBI36
NG_011811.2:g.7608_7611delinsCATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.149_152delinsCATG
ENST00000482662.2:n.411+19_411+22delinsCATG
ENST00000496962.2:c.363_366delinsCATG ENSP00000508856.1:p.Ile121=
ENST00000685865.1:n.455_458delinsCATG
ENST00000687250.1:n.466_469delinsCATG
ENST00000687995.1:n.404_407delinsCATG
ENST00000688205.1:c.363_366delinsCATG ENSP00000509673.1:p.Ile121=
ENST00000688788.1:n.455_458delinsCATG
ENST00000689276.1:c.344+19_344+22delinsCATG ENSP00000510012.1:n.344+19_344+22delinsCATG
ENST00000689576.1:c.363_366delinsCATG ENSP00000508712.1:p.Ile121=
ENST00000690108.1:c.344+19_344+22delinsCATG ENSP00000510617.1:n.344+19_344+22delinsCATG
ENST00000690468.1:c.173+19_173+22delinsCATG ENSP00000509078.1:n.173+19_173+22delinsCATG
ENST00000690595.1:c.214+1888_214+1891delinsCATG ENSP00000508979.1:n.214+1888_214+1891delinsCATG
ENST00000691348.1:c.192_195delinsCATG ENSP00000509369.1:p.Ile64=
ENST00000691410.1:c.344+19_344+22delinsCATG ENSP00000508479.1:n.344+19_344+22delinsCATG
ENST00000693287.1:c.-67+2459_-67+2462delinsCATG ENSP00000510264.1:n.-67+2459_-67+2462delinsCATG
ENST00000693681.1:c.192_195delinsCATG ENSP00000510789.1:p.Ile64=
ENST00000233838.9:c.363_366delinsCATG MANE Select ENSP00000233838.3:p.Ile121=
ENST00000233838.8:c.363_366delinsCATG ENSP00000233838.3:p.Ile121=
ENST00000421496.5:c.173+19_173+22delinsCATG ENSP00000400384.1:n.173+19_173+22delinsCATG
ENST00000423570.5:c.344+19_344+22delinsCATG ENSP00000389426.1:n.344+19_344+22delinsCATG
ENST00000428479.3:c.192_195delinsCATG ENSP00000390748.3:p.Ile64=
ENST00000430215.7:c.192_195delinsCATG ENSP00000408045.3:p.Ile64=
ENST00000465637.5:n.178+79_178+82delinsCATG
ENST00000481541.1:n.257_260delinsCATG
ENST00000496962.1:n.482_485delinsCATG
NM_000821.5:c.363_366delinsCATG NP_000812.2:p.Ile121=
NM_000821.6:c.363_366delinsCATG NP_000812.2:p.Ile121=
NM_001142269.2:c.192_195delinsCATG NP_001135741.1:p.Ile64=
NM_001142269.3:c.192_195delinsCATG NP_001135741.1:p.Ile64=
NM_001311312.1:c.363_366delinsCATG NP_001298241.1:p.Ile121=
XM_005264259.3:c.363_366delinsCATG XP_005264316.1:p.Ile121=
XM_011532764.1:c.-296_-293delinsCATG XP_011531066.1:n.-296_-293delinsCATG
XM_011532765.1:c.-296_-293delinsCATG XP_011531067.1:n.-296_-293delinsCATG
XR_939677.1:n.428_431delinsCATG
XM_005264259.5:c.363_366delinsCATG XP_005264316.1:p.Ile121=
XM_011532764.3:c.-296_-293delinsCATG XP_011531066.1:n.-296_-293delinsCATG
XM_011532765.3:c.-296_-293delinsCATG XP_011531067.1:n.-296_-293delinsCATG
XM_017003803.2:c.192_195delinsCATG XP_016859292.1:p.Ile64=
XR_001738703.2:n.428_431delinsCATG
NM_000821.7:c.363_366delinsCATG MANE Select NP_000812.2:p.Ile121=
NM_001142269.4:c.192_195delinsCATG NP_001135741.1:p.Ile64=
NM_001311312.2:c.363_366delinsCATG NP_001298241.1:p.Ile121=