Canonical Allele Identifier: CA1881272026
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130480449G= , CM000671.2:g.130480449G= GRCh38
NC_000009.11:g.133355836G= , CM000671.1:g.133355836G= GRCh37
NC_000009.10:g.132345657G= NCBI36
NG_011542.1:g.40743G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.838G= MANE Select ENSP00000253004.6:p.Gly280=
ENST00000352480.9:c.838G= ENSP00000253004.6:p.Gly280=
ENST00000372386.6:n.109G=
ENST00000372393.7:c.838G= ENSP00000361469.2:p.Gly280=
ENST00000372394.5:c.838G= ENSP00000361471.1:p.Gly280=
ENST00000470849.4:n.563G=
ENST00000492400.5:n.347G=
ENST00000493984.6:n.615G=
NM_000050.4:c.838G= NP_000041.2:p.Gly280=
NM_054012.3:c.838G= NP_446464.1:p.Gly280=
XM_005272200.2:c.838G= XP_005272257.1:p.Gly280=
XM_011518705.1:c.952G= XP_011517007.1:p.Gly318=
XM_005272200.3:c.838G= XP_005272257.1:p.Gly280=
XM_011518705.2:c.952G= XP_011517007.1:p.Gly318=
XM_017014729.1:c.934G= XP_016870218.1:p.Gly312=
NM_054012.4:c.838G= MANE Select NP_446464.1:p.Gly280=