Canonical Allele Identifier: CA1266819920
Gene: GGCX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85545883_85545887delinsGATAA , CM000664.2:g.85545883_85545887delinsGATAA GRCh38
NC_000002.11:g.85773006_85773010delinsGATAA , CM000664.1:g.85773006_85773010delinsGATAA GRCh37
NC_000002.10:g.85626517_85626521delinsGATAA NCBI36
NG_011811.2:g.20648_20652delinsTTATC
NG_029183.1:g.11906_11910delinsGATAA

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*4047_*4051delinsTTATC MANE Select ENSP00000233838.3:n.*4047_*4051delinsTTATC
ENST00000233838.8:c.*4047_*4051delinsTTATC ENSP00000233838.3:n.*4047_*4051delinsTTATC
NM_000821.5:c.*4047_*4051delinsTTATC NP_000812.2:n.*4047_*4051delinsTTATC
NM_000821.6:c.*4047_*4051delinsTTATC NP_000812.2:n.*4047_*4051delinsTTATC
NM_001142269.2:c.*4047_*4051delinsTTATC NP_001135741.1:n.*4047_*4051delinsTTATC
NM_001142269.3:c.*4047_*4051delinsTTATC NP_001135741.1:n.*4047_*4051delinsTTATC
NM_000821.7:c.*4047_*4051delinsTTATC MANE Select NP_000812.2:n.*4047_*4051delinsTTATC
NM_001142269.4:c.*4047_*4051delinsTTATC NP_001135741.1:n.*4047_*4051delinsTTATC
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