Canonical Allele Identifier: CA1266819996
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85545961_85545963delinsATC , CM000664.2:g.85545961_85545963delinsATC GRCh38
NC_000002.11:g.85773084_85773086delinsATC , CM000664.1:g.85773084_85773086delinsATC GRCh37
NC_000002.10:g.85626595_85626597delinsATC NCBI36
NG_011811.2:g.20572_20574delinsGAT
NG_029183.1:g.11984_11986delinsATC

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*3971_*3973delinsGAT MANE Select ENSP00000233838.3:n.*3971_*3973delinsGAT
ENST00000233838.8:c.*3971_*3973delinsGAT ENSP00000233838.3:n.*3971_*3973delinsGAT
NM_000821.5:c.*3971_*3973delinsGAT NP_000812.2:n.*3971_*3973delinsGAT
NM_000821.6:c.*3971_*3973delinsGAT NP_000812.2:n.*3971_*3973delinsGAT
NM_001142269.2:c.*3971_*3973delinsGAT NP_001135741.1:n.*3971_*3973delinsGAT
NM_001142269.3:c.*3971_*3973delinsGAT NP_001135741.1:n.*3971_*3973delinsGAT
NM_000821.7:c.*3971_*3973delinsGAT MANE Select NP_000812.2:n.*3971_*3973delinsGAT
NM_001142269.4:c.*3971_*3973delinsGAT NP_001135741.1:n.*3971_*3973delinsGAT