Canonical Allele Identifier: CA1266820721
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546404_85546408delinsCAGAG , CM000664.2:g.85546404_85546408delinsCAGAG GRCh38
NC_000002.11:g.85773527_85773531delinsCAGAG , CM000664.1:g.85773527_85773531delinsCAGAG GRCh37
NC_000002.10:g.85627038_85627042delinsCAGAG NCBI36
NG_011811.2:g.20127_20131delinsCTCTG
NG_029183.1:g.12427_12431delinsCAGAG

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*3526_*3530delinsCTCTG MANE Select ENSP00000233838.3:n.*3526_*3530delinsCTCT...
ENST00000233838.8:c.*3526_*3530delinsCTCTG ENSP00000233838.3:n.*3526_*3530delinsCTCT...
NM_000821.5:c.*3526_*3530delinsCTCTG NP_000812.2:n.*3526_*3530delinsCTCTG
NM_000821.6:c.*3526_*3530delinsCTCTG NP_000812.2:n.*3526_*3530delinsCTCTG
NM_001142269.2:c.*3526_*3530delinsCTCTG NP_001135741.1:n.*3526_*3530delinsCTCTG
NM_001142269.3:c.*3526_*3530delinsCTCTG NP_001135741.1:n.*3526_*3530delinsCTCTG
NM_000821.7:c.*3526_*3530delinsCTCTG MANE Select NP_000812.2:n.*3526_*3530delinsCTCTG
NM_001142269.4:c.*3526_*3530delinsCTCTG NP_001135741.1:n.*3526_*3530delinsCTCTG