Canonical Allele Identifier: CA200617791
Gene: ASS1 HGNC NCBI

Linked Data

dbSNP Id: rs560065283

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130471424G>A , CM000671.2:g.130471424G>A GRCh38
NC_000009.11:g.133346811G>A , CM000671.1:g.133346811G>A GRCh37
NC_000009.10:g.132336632G>A NCBI36
NG_011542.1:g.31718G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.567-61G>A MANE Select ENSP00000253004.6:n.567-61G>A
ENST00000352480.9:c.567-61G>A ENSP00000253004.6:n.567-61G>A
ENST00000372393.7:c.567-61G>A ENSP00000361469.2:n.567-61G>A
ENST00000372394.5:c.567-61G>A ENSP00000361471.1:n.567-61G>A
ENST00000422569.5:c.567-61G>A ENSP00000394212.1:n.567-61G>A
ENST00000443588.1:c.510-61G>A ENSP00000397785.1:n.510-61G>A
ENST00000467695.5:n.276-61G>A
ENST00000493984.6:n.398-61G>A
NM_000050.4:c.567-61G>A NP_000041.2:n.567-61G>A
NM_054012.3:c.567-61G>A NP_446464.1:n.567-61G>A
XM_005272200.2:c.567-61G>A XP_005272257.1:n.567-61G>A
XM_011518705.1:c.681-61G>A XP_011517007.1:n.681-61G>A
XM_005272200.3:c.567-61G>A XP_005272257.1:n.567-61G>A
XM_011518705.2:c.681-61G>A XP_011517007.1:n.681-61G>A
XM_017014729.1:c.663-61G>A XP_016870218.1:n.663-61G>A
NM_054012.4:c.567-61G>A MANE Select NP_446464.1:n.567-61G>A