Canonical Allele Identifier: CA2750761906
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85558998_85558999insCCCACCAAACAC , CM000664.2:g.85558998_85558999insCCCACCAAACAC GRCh38
NC_000002.11:g.85786121_85786122insCCCACCAAACAC , CM000664.1:g.85786121_85786122insCCCACCAAACAC GRCh37
NC_000002.10:g.85639632_85639633insCCCACCAAACAC NCBI36
NG_011811.2:g.7540_7541insTTGGTGGGGTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.81_82insTTGGTGGGGTGT
ENST00000482662.2:n.362_363insTTGGTGGGGTGT
ENST00000496962.2:c.295_296insTTGGTGGGGTGT ENSP00000508856.1:p.Val98_Cys99insPheGlyGlyVal
ENST00000685865.1:n.387_388insTTGGTGGGGTGT
ENST00000687250.1:n.398_399insTTGGTGGGGTGT
ENST00000687995.1:n.336_337insTTGGTGGGGTGT
ENST00000688205.1:c.295_296insTTGGTGGGGTGT ENSP00000509673.1:p.Val98_Cys99insPheGlyGlyVal
ENST00000688788.1:n.387_388insTTGGTGGGGTGT
ENST00000689276.1:c.295_296insTTGGTGGGGTGT ENSP00000510012.1:p.Val98_Cys99insPheGlyGlyVal
ENST00000689576.1:c.295_296insTTGGTGGGGTGT ENSP00000508712.1:p.Val98_Cys99insPheGlyGlyVal
ENST00000690108.1:c.295_296insTTGGTGGGGTGT ENSP00000510617.1:p.Val98_Cys99insPheGlyGlyVal
ENST00000690468.1:c.124_125insTTGGTGGGGTGT ENSP00000509078.1:p.Val41_Cys42insPheGlyGlyVal
ENST00000690595.1:c.214+1820_214+1821insTTGGTGGGGTGT ENSP00000508979.1:n.214+1820_214+1821insTTGGTGGGGTGT
ENST00000691348.1:c.124_125insTTGGTGGGGTGT ENSP00000509369.1:p.Val41_Cys42insPheGlyGlyVal
ENST00000691410.1:c.295_296insTTGGTGGGGTGT ENSP00000508479.1:p.Val98_Cys99insPheGlyGlyVal
ENST00000693287.1:c.-67+2391_-67+2392insTTGGTGGGGTGT ENSP00000510264.1:n.-67+2391_-67+2392insTTGGTGGGGTGT
ENST00000693681.1:c.124_125insTTGGTGGGGTGT ENSP00000510789.1:p.Val41_Cys42insPheGlyGlyVal
ENST00000233838.9:c.295_296insTTGGTGGGGTGT MANE Select ENSP00000233838.3:p.Val98_Cys99insPheGlyGlyVal
ENST00000233838.8:c.295_296insTTGGTGGGGTGT ENSP00000233838.3:p.Val98_Cys99insPheGlyGlyVal
ENST00000421496.5:c.124_125insTTGGTGGGGTGT ENSP00000400384.1:p.Val41_Cys42insPheGlyGlyVal
ENST00000423570.5:c.295_296insTTGGTGGGGTGT ENSP00000389426.1:p.Val98_Cys99insPheGlyGlyVal
ENST00000428479.3:c.124_125insTTGGTGGGGTGT ENSP00000390748.3:p.Val41_Cys42insPheGlyGlyVal
ENST00000430215.7:c.124_125insTTGGTGGGGTGT ENSP00000408045.3:p.Val41_Cys42insPheGlyGlyVal
ENST00000465637.5:n.178+11_178+12insTTGGTGGGGTGT
ENST00000481541.1:n.189_190insTTGGTGGGGTGT
ENST00000496962.1:n.414_415insTTGGTGGGGTGT
NM_000821.5:c.295_296insTTGGTGGGGTGT NP_000812.2:p.Val98_Cys99insPheGlyGlyVal
NM_000821.6:c.295_296insTTGGTGGGGTGT NP_000812.2:p.Val98_Cys99insPheGlyGlyVal
NM_001142269.2:c.124_125insTTGGTGGGGTGT NP_001135741.1:p.Val41_Cys42insPheGlyGlyVal
NM_001142269.3:c.124_125insTTGGTGGGGTGT NP_001135741.1:p.Val41_Cys42insPheGlyGlyVal
NM_001311312.1:c.295_296insTTGGTGGGGTGT NP_001298241.1:p.Val98_Cys99insPheGlyGlyVal
XM_005264259.3:c.295_296insTTGGTGGGGTGT XP_005264316.1:p.Val98_Cys99insPheGlyGlyVal
XM_011532764.1:c.-364_-363insTTGGTGGGGTGT XP_011531066.1:n.-364_-363insTTGGTGGGGTGT
XM_011532765.1:c.-364_-363insTTGGTGGGGTGT XP_011531067.1:n.-364_-363insTTGGTGGGGTGT
XR_939677.1:n.360_361insTTGGTGGGGTGT
XM_005264259.5:c.295_296insTTGGTGGGGTGT XP_005264316.1:p.Val98_Cys99insPheGlyGlyVal
XM_011532764.3:c.-364_-363insTTGGTGGGGTGT XP_011531066.1:n.-364_-363insTTGGTGGGGTGT
XM_011532765.3:c.-364_-363insTTGGTGGGGTGT XP_011531067.1:n.-364_-363insTTGGTGGGGTGT
XM_017003803.2:c.124_125insTTGGTGGGGTGT XP_016859292.1:p.Val41_Cys42insPheGlyGlyVal
XR_001738703.2:n.360_361insTTGGTGGGGTGT
NM_000821.7:c.295_296insTTGGTGGGGTGT MANE Select NP_000812.2:p.Val98_Cys99insPheGlyGlyVal
NM_001142269.4:c.124_125insTTGGTGGGGTGT NP_001135741.1:p.Val41_Cys42insPheGlyGlyVal
NM_001311312.2:c.295_296insTTGGTGGGGTGT NP_001298241.1:p.Val98_Cys99insPheGlyGlyVal