Canonical Allele Identifier: CA2845030465
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85558965_85558966insCT , CM000664.2:g.85558965_85558966insCT GRCh38
NC_000002.11:g.85786088_85786089insCT , CM000664.1:g.85786088_85786089insCT GRCh37
NC_000002.10:g.85639599_85639600insCT NCBI36
NG_011811.2:g.7569_7570insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.110_111insAG
ENST00000482662.2:n.391_392insAG
ENST00000496962.2:c.324_325insAG ENSP00000508856.1:p.Pro109SerfsTer?
ENST00000685865.1:n.416_417insAG
ENST00000687250.1:n.427_428insAG
ENST00000687995.1:n.365_366insAG
ENST00000688205.1:c.324_325insAG ENSP00000509673.1:p.Pro109SerfsTer22
ENST00000688788.1:n.416_417insAG
ENST00000689276.1:c.324_325insAG ENSP00000510012.1:p.Pro109SerfsTer?
ENST00000689576.1:c.324_325insAG ENSP00000508712.1:p.Pro109SerfsTer22
ENST00000690108.1:c.324_325insAG ENSP00000510617.1:p.Pro109SerfsTer14
ENST00000690468.1:c.153_154insAG ENSP00000509078.1:p.Pro52SerfsTer?
ENST00000690595.1:c.214+1849_214+1850insAG ENSP00000508979.1:n.214+1849_214+1850insAG
ENST00000691348.1:c.153_154insAG ENSP00000509369.1:p.Pro52SerfsTer22
ENST00000691410.1:c.324_325insAG ENSP00000508479.1:p.Pro109SerfsTer14
ENST00000693287.1:c.-67+2420_-67+2421insAG ENSP00000510264.1:n.-67+2420_-67+2421insAG
ENST00000693681.1:c.153_154insAG ENSP00000510789.1:p.Pro52SerfsTer?
ENST00000233838.9:c.324_325insAG MANE Select ENSP00000233838.3:p.Pro109SerfsTer22
ENST00000233838.8:c.324_325insAG ENSP00000233838.3:p.Pro109SerfsTer22
ENST00000421496.5:c.153_154insAG ENSP00000400384.1:p.Pro52SerfsTer14
ENST00000423570.5:c.324_325insAG ENSP00000389426.1:p.Pro109SerfsTer14
ENST00000428479.3:c.153_154insAG ENSP00000390748.3:p.Pro52SerfsTer29
ENST00000430215.7:c.153_154insAG ENSP00000408045.3:p.Pro52SerfsTer22
ENST00000465637.5:n.178+40_178+41insAG
ENST00000481541.1:n.218_219insAG
ENST00000496962.1:n.443_444insAG
NM_000821.5:c.324_325insAG NP_000812.2:p.Pro109SerfsTer22
NM_000821.6:c.324_325insAG NP_000812.2:p.Pro109SerfsTer22
NM_001142269.2:c.153_154insAG NP_001135741.1:p.Pro52SerfsTer22
NM_001142269.3:c.153_154insAG NP_001135741.1:p.Pro52SerfsTer22
NM_001311312.1:c.324_325insAG NP_001298241.1:p.Pro109SerfsTer?
XM_005264259.3:c.324_325insAG XP_005264316.1:p.Pro109SerfsTer22
XM_011532764.1:c.-335_-334insAG XP_011531066.1:n.-335_-334insAG
XM_011532765.1:c.-335_-334insAG XP_011531067.1:n.-335_-334insAG
XR_939677.1:n.389_390insAG
XM_005264259.5:c.324_325insAG XP_005264316.1:p.Pro109SerfsTer22
XM_011532764.3:c.-335_-334insAG XP_011531066.1:n.-335_-334insAG
XM_011532765.3:c.-335_-334insAG XP_011531067.1:n.-335_-334insAG
XM_017003803.2:c.153_154insAG XP_016859292.1:p.Pro52SerfsTer22
XR_001738703.2:n.389_390insAG
NM_000821.7:c.324_325insAG MANE Select NP_000812.2:p.Pro109SerfsTer22
NM_001142269.4:c.153_154insAG NP_001135741.1:p.Pro52SerfsTer22
NM_001311312.2:c.324_325insAG NP_001298241.1:p.Pro109SerfsTer?