Canonical Allele Identifier: CA253834
Gene: ASS1 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.130499545G>A
GRCh37 chr9:g.133374932G>A
Revel Score:
ENST00000334909 0.967
ENST00000352480 (MANE Select) 0.967
ENST00000372394 0.967
ENST00000372393 0.967
ENST00000372386 0.967
gnomAD v2:
9:133374932 G / A
gnomAD v3:
9:130499545 G / A
gnomAD v4:
chr9-130499545-G-A
Joint Max Group AF 0.00077399 (SAS)
Genomes Max Group AF 0.00032945 (NFE)
Exomes Max Group AF 0.00078532 (SAS)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130499545G>A , CM000671.2:g.130499545G>A GRCh38
NC_000009.11:g.133374932G>A , CM000671.1:g.133374932G>A GRCh37
NC_000009.10:g.132364753G>A NCBI36
NG_011542.1:g.59839G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.1168G>A MANE Select ENSP00000253004.6:p.Gly390Arg
ENST00000352480.9:c.1168G>A ENSP00000253004.6:p.Gly390Arg
ENST00000372386.6:n.439G>A
ENST00000372393.7:c.1168G>A ENSP00000361469.2:p.Gly390Arg
ENST00000372394.5:c.1168G>A ENSP00000361471.1:p.Gly390Arg
NM_000050.4:c.1168G>A NP_000041.2:p.Gly390Arg
NM_054012.3:c.1168G>A NP_446464.1:p.Gly390Arg
XM_005272200.2:c.1168G>A XP_005272257.1:p.Gly390Arg
XM_011518705.1:c.1282G>A XP_011517007.1:p.Gly428Arg
XR_930393.1:n.1059+402C>T
XM_005272200.3:c.1168G>A XP_005272257.1:p.Gly390Arg
XM_011518705.2:c.1282G>A XP_011517007.1:p.Gly428Arg
XM_017014729.1:c.1264G>A XP_016870218.1:p.Gly422Arg
XR_930393.2:n.1101+402C>T
NM_054012.4:c.1168G>A MANE Select NP_446464.1:p.Gly390Arg
Search 100 bp 5'
Search 100 bp 3'