Canonical Allele Identifier: CA1881276618
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130489347C= , CM000671.2:g.130489347C= GRCh38
NC_000009.11:g.133364734C= , CM000671.1:g.133364734C= GRCh37
NC_000009.10:g.132354555C= NCBI36
NG_011542.1:g.49641C=

Transcript Alleles

HGVS Amino-acid change
ENST00000352480.10:c.853C= MANE Select ENSP00000253004.6:p.Pro285=
ENST00000352480.9:c.853C= ENSP00000253004.6:p.Pro285=
ENST00000372386.6:n.124C=
ENST00000372393.7:c.853C= ENSP00000361469.2:p.Pro285=
ENST00000372394.5:c.853C= ENSP00000361471.1:p.Pro285=
ENST00000470849.4:n.578C=
ENST00000492400.5:n.362C=
ENST00000493984.6:n.630C=
NM_000050.4:c.853C= NP_000041.2:p.Pro285=
NM_054012.3:c.853C= NP_446464.1:p.Pro285=
XM_005272200.2:c.853C= XP_005272257.1:p.Pro285=
XM_011518705.1:c.967C= XP_011517007.1:p.Pro323=
XM_005272200.3:c.853C= XP_005272257.1:p.Pro285=
XM_011518705.2:c.967C= XP_011517007.1:p.Pro323=
XM_017014729.1:c.949C= XP_016870218.1:p.Pro317=
NM_054012.4:c.853C= MANE Select NP_446464.1:p.Pro285=