Canonical Allele Identifier: CA894034969

Gene: GGCX

Linked Data

• dbSNP Id: rs1326363476
• MyVariant Identifiers: chr2:g.85773657_85773659del (hg19) ; chr2:g.85546534_85546536del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85546534_85546536del , CM000664.2:g.85546534_85546536del	GRCh38
NC_000002.11:g.85773657_85773659del , CM000664.1:g.85773657_85773659del	GRCh37
NC_000002.10:g.85627168_85627170del	NCBI36
NG_011811.2:g.19999_20001del
NG_029183.1:g.12557_12559del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233838.9:c.*3398_*3400del MANE Select	ENSP00000233838.3:n.*3398_*3400del
ENST00000233838.8:c.*3398_*3400del	ENSP00000233838.3:n.*3398_*3400del
NM_000821.5:c.*3398_*3400del	NP_000812.2:n.*3398_*3400del
NM_000821.6:c.*3398_*3400del	NP_000812.2:n.*3398_*3400del
NM_001142269.2:c.*3398_*3400del	NP_001135741.1:n.*3398_*3400del
NM_001142269.3:c.*3398_*3400del	NP_001135741.1:n.*3398_*3400del
NM_000821.7:c.*3398_*3400del MANE Select	NP_000812.2:n.*3398_*3400del
NM_001142269.4:c.*3398_*3400del	NP_001135741.1:n.*3398_*3400del