Canonical Allele Identifier: CA894034802

Gene: GGCX

Linked Data

• dbSNP Id: rs1370481501
• MyVariant Identifiers: chr2:g.85773528_85773531del (hg19) ; chr2:g.85546405_85546408del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85546405_85546408del , CM000664.2:g.85546405_85546408del	GRCh38
NC_000002.11:g.85773528_85773531del , CM000664.1:g.85773528_85773531del	GRCh37
NC_000002.10:g.85627039_85627042del	NCBI36
NG_011811.2:g.20127_20130del
NG_029183.1:g.12428_12431del

Transcript Alleles

HGVS	Amino-acid change
ENST00000233838.9:c.*3526_*3529del MANE Select	ENSP00000233838.3:n.*3526_*3529del
ENST00000233838.8:c.*3526_*3529del	ENSP00000233838.3:n.*3526_*3529del
NM_000821.5:c.*3526_*3529del	NP_000812.2:n.*3526_*3529del
NM_000821.6:c.*3526_*3529del	NP_000812.2:n.*3526_*3529del
NM_001142269.2:c.*3526_*3529del	NP_001135741.1:n.*3526_*3529del
NM_001142269.3:c.*3526_*3529del	NP_001135741.1:n.*3526_*3529del
NM_000821.7:c.*3526_*3529del MANE Select	NP_000812.2:n.*3526_*3529del
NM_001142269.4:c.*3526_*3529del	NP_001135741.1:n.*3526_*3529del