Canonical Allele Identifier: CA1266821491

Gene: GGCX

Linked Data

• dbSNP Id: rs1691696411

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85546943_85546945del , CM000664.2:g.85546943_85546945del	GRCh38
NC_000002.11:g.85774066_85774068del , CM000664.1:g.85774066_85774068del	GRCh37
NC_000002.10:g.85627577_85627579del	NCBI36
NG_011811.2:g.19592_19594del
NG_029183.1:g.12966_12968del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233838.9:c.*2991_*2993del MANE Select	ENSP00000233838.3:n.*2991_*2993del
ENST00000233838.8:c.*2991_*2993del	ENSP00000233838.3:n.*2991_*2993del
NM_000821.5:c.*2991_*2993del	NP_000812.2:n.*2991_*2993del
NM_000821.6:c.*2991_*2993del	NP_000812.2:n.*2991_*2993del
NM_001142269.2:c.*2991_*2993del	NP_001135741.1:n.*2991_*2993del
NM_001142269.3:c.*2991_*2993del	NP_001135741.1:n.*2991_*2993del
NM_000821.7:c.*2991_*2993del MANE Select	NP_000812.2:n.*2991_*2993del
NM_001142269.4:c.*2991_*2993del	NP_001135741.1:n.*2991_*2993del