Canonical Allele Identifier: CA894035199

Gene: GGCX

Linked Data

• dbSNP Id: rs1453908086
• gnomAD v3: 2-85546780-CAA-C
• gnomAD v4: 2-85546780-CAA-C
• MyVariant Identifiers: chr2:g.85773904_85773905del (hg19) ; chr2:g.85546781_85546782del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85546781_85546782del , CM000664.2:g.85546781_85546782del	GRCh38
NC_000002.11:g.85773904_85773905del , CM000664.1:g.85773904_85773905del	GRCh37
NC_000002.10:g.85627415_85627416del	NCBI36
NG_011811.2:g.19753_19754del
NG_029183.1:g.12804_12805del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233838.9:c.*3152_*3153del MANE Select	ENSP00000233838.3:n.*3152_*3153del
ENST00000233838.8:c.*3152_*3153del	ENSP00000233838.3:n.*3152_*3153del
NM_000821.5:c.*3152_*3153del	NP_000812.2:n.*3152_*3153del
NM_000821.6:c.*3152_*3153del	NP_000812.2:n.*3152_*3153del
NM_001142269.2:c.*3152_*3153del	NP_001135741.1:n.*3152_*3153del
NM_001142269.3:c.*3152_*3153del	NP_001135741.1:n.*3152_*3153del
NM_000821.7:c.*3152_*3153del MANE Select	NP_000812.2:n.*3152_*3153del
NM_001142269.4:c.*3152_*3153del	NP_001135741.1:n.*3152_*3153del