Canonical Allele Identifier: CA2659853401
Gene: GGCX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85547881del , CM000664.2:g.85547881del GRCh38
NC_000002.11:g.85775004del , CM000664.1:g.85775004del GRCh37
NC_000002.10:g.85628515del NCBI36
NG_011811.2:g.18654del

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*2053del MANE Select ENSP00000233838.3:n.*2053del
ENST00000233838.8:c.*2053del ENSP00000233838.3:n.*2053del
ENST00000465637.5:n.302del
NM_000821.5:c.*2053del NP_000812.2:n.*2053del
NM_000821.6:c.*2053del NP_000812.2:n.*2053del
NM_001142269.2:c.*2053del NP_001135741.1:n.*2053del
NM_001142269.3:c.*2053del NP_001135741.1:n.*2053del
NM_000821.7:c.*2053del MANE Select NP_000812.2:n.*2053del
NM_001142269.4:c.*2053del NP_001135741.1:n.*2053del