Canonical Allele Identifier: CA534171613
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs1199059205

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85545969dup , CM000664.2:g.85545969dup GRCh38
NC_000002.11:g.85773092dup , CM000664.1:g.85773092dup GRCh37
NC_000002.10:g.85626603dup NCBI36
NG_011811.2:g.20566dup
NG_029183.1:g.11992dup

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*3965dup MANE Select ENSP00000233838.3:n.*3965dup
ENST00000233838.8:c.*3965dup ENSP00000233838.3:n.*3965dup
NM_000821.5:c.*3965dup NP_000812.2:n.*3965dup
NM_000821.6:c.*3965dup NP_000812.2:n.*3965dup
NM_001142269.2:c.*3965dup NP_001135741.1:n.*3965dup
NM_001142269.3:c.*3965dup NP_001135741.1:n.*3965dup
NM_000821.7:c.*3965dup MANE Select NP_000812.2:n.*3965dup
NM_001142269.4:c.*3965dup NP_001135741.1:n.*3965dup