Canonical Allele Identifier: CA1266819762

Gene: GGCX

Linked Data

• dbSNP Id: rs1691629038

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85545748del , CM000664.2:g.85545748del	GRCh38
NC_000002.11:g.85772871del , CM000664.1:g.85772871del	GRCh37
NC_000002.10:g.85626382del	NCBI36
NG_011811.2:g.20787del
NG_029183.1:g.11771del

Transcript Alleles

HGVS	Amino-acid change
ENST00000233838.9:c.*4186del MANE Select	ENSP00000233838.3:n.*4186del
ENST00000233838.8:c.*4186del	ENSP00000233838.3:n.*4186del
NM_000821.5:c.*4186del	NP_000812.2:n.*4186del
NM_000821.6:c.*4186del	NP_000812.2:n.*4186del
NM_001142269.2:c.*4186del	NP_001135741.1:n.*4186del
NM_001142269.3:c.*4186del	NP_001135741.1:n.*4186del
NM_000821.7:c.*4186del MANE Select	NP_000812.2:n.*4186del
NM_001142269.4:c.*4186del	NP_001135741.1:n.*4186del