Canonical Allele Identifier: CA2659853411
Gene: GGCX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85547899_85547911del , CM000664.2:g.85547899_85547911del GRCh38
NC_000002.11:g.85775022_85775034del , CM000664.1:g.85775022_85775034del GRCh37
NC_000002.10:g.85628533_85628545del NCBI36
NG_011811.2:g.18624_18636del

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*2023_*2035del MANE Select ENSP00000233838.3:n.*2023_*2035del
ENST00000233838.8:c.*2023_*2035del ENSP00000233838.3:n.*2023_*2035del
ENST00000465637.5:n.272_284del
NM_000821.5:c.*2023_*2035del NP_000812.2:n.*2023_*2035del
NM_000821.6:c.*2023_*2035del NP_000812.2:n.*2023_*2035del
NM_001142269.2:c.*2023_*2035del NP_001135741.1:n.*2023_*2035del
NM_001142269.3:c.*2023_*2035del NP_001135741.1:n.*2023_*2035del
NM_000821.7:c.*2023_*2035del MANE Select NP_000812.2:n.*2023_*2035del
NM_001142269.4:c.*2023_*2035del NP_001135741.1:n.*2023_*2035del