Canonical Allele Identifier: CA1881276612
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130489334T= , CM000671.2:g.130489334T= GRCh38
NC_000009.11:g.133364721T= , CM000671.1:g.133364721T= GRCh37
NC_000009.10:g.132354542T= NCBI36
NG_011542.1:g.49628T=

Transcript Alleles

HGVS Amino-acid change
ENST00000352480.10:c.840T= MANE Select ENSP00000253004.6:p.Gly280=
ENST00000352480.9:c.840T= ENSP00000253004.6:p.Gly280=
ENST00000372386.6:n.111T=
ENST00000372393.7:c.840T= ENSP00000361469.2:p.Gly280=
ENST00000372394.5:c.840T= ENSP00000361471.1:p.Gly280=
ENST00000470849.4:n.565T=
ENST00000492400.5:n.349T=
ENST00000493984.6:n.617T=
NM_000050.4:c.840T= NP_000041.2:p.Gly280=
NM_054012.3:c.840T= NP_446464.1:p.Gly280=
XM_005272200.2:c.840T= XP_005272257.1:p.Gly280=
XM_011518705.1:c.954T= XP_011517007.1:p.Gly318=
XM_005272200.3:c.840T= XP_005272257.1:p.Gly280=
XM_011518705.2:c.954T= XP_011517007.1:p.Gly318=
XM_017014729.1:c.936T= XP_016870218.1:p.Gly312=
NM_054012.4:c.840T= MANE Select NP_446464.1:p.Gly280=