Canonical Allele Identifier: CA1266820710
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546402_85546404delinsAAC , CM000664.2:g.85546402_85546404delinsAAC GRCh38
NC_000002.11:g.85773525_85773527delinsAAC , CM000664.1:g.85773525_85773527delinsAAC GRCh37
NC_000002.10:g.85627036_85627038delinsAAC NCBI36
NG_011811.2:g.20131_20133delinsGTT
NG_029183.1:g.12425_12427delinsAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*3530_*3532delinsGTT MANE Select ENSP00000233838.3:n.*3530_*3532delinsGTT
ENST00000233838.8:c.*3530_*3532delinsGTT ENSP00000233838.3:n.*3530_*3532delinsGTT
NM_000821.5:c.*3530_*3532delinsGTT NP_000812.2:n.*3530_*3532delinsGTT
NM_000821.6:c.*3530_*3532delinsGTT NP_000812.2:n.*3530_*3532delinsGTT
NM_001142269.2:c.*3530_*3532delinsGTT NP_001135741.1:n.*3530_*3532delinsGTT
NM_001142269.3:c.*3530_*3532delinsGTT NP_001135741.1:n.*3530_*3532delinsGTT
NM_000821.7:c.*3530_*3532delinsGTT MANE Select NP_000812.2:n.*3530_*3532delinsGTT
NM_001142269.4:c.*3530_*3532delinsGTT NP_001135741.1:n.*3530_*3532delinsGTT