Canonical Allele Identifier: CA2659852278

Gene: GGCX

Linked Data

• gnomAD v4: 2-85545879-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85545879C>A , CM000664.2:g.85545879C>A	GRCh38
NC_000002.11:g.85773002C>A , CM000664.1:g.85773002C>A	GRCh37
NC_000002.10:g.85626513C>A	NCBI36
NG_011811.2:g.20656G>T
NG_029183.1:g.11902C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233838.9:c.*4055G>T MANE Select	ENSP00000233838.3:n.*4055G>T
ENST00000233838.8:c.*4055G>T	ENSP00000233838.3:n.*4055G>T
NM_000821.5:c.*4055G>T	NP_000812.2:n.*4055G>T
NM_000821.6:c.*4055G>T	NP_000812.2:n.*4055G>T
NM_001142269.2:c.*4055G>T	NP_001135741.1:n.*4055G>T
NM_001142269.3:c.*4055G>T	NP_001135741.1:n.*4055G>T
NM_000821.7:c.*4055G>T MANE Select	NP_000812.2:n.*4055G>T
NM_001142269.4:c.*4055G>T	NP_001135741.1:n.*4055G>T