Canonical Allele Identifier: CA1881276609
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130489326T= , CM000671.2:g.130489326T= GRCh38
NC_000009.11:g.133364713T= , CM000671.1:g.133364713T= GRCh37
NC_000009.10:g.132354534T= NCBI36
NG_011542.1:g.49620T=

Transcript Alleles

HGVS Amino-acid change
ENST00000352480.10:c.839-7T= MANE Select ENSP00000253004.6:n.839-7T=
ENST00000352480.9:c.839-7T= ENSP00000253004.6:n.839-7T=
ENST00000372386.6:n.110-7T=
ENST00000372393.7:c.839-7T= ENSP00000361469.2:n.839-7T=
ENST00000372394.5:c.839-7T= ENSP00000361471.1:n.839-7T=
ENST00000470849.4:n.564-7T=
ENST00000492400.5:n.348-7T=
ENST00000493984.6:n.616-7T=
NM_000050.4:c.839-7T= NP_000041.2:n.839-7T=
NM_054012.3:c.839-7T= NP_446464.1:n.839-7T=
XM_005272200.2:c.839-7T= XP_005272257.1:n.839-7T=
XM_011518705.1:c.953-7T= XP_011517007.1:n.953-7T=
XM_005272200.3:c.839-7T= XP_005272257.1:n.839-7T=
XM_011518705.2:c.953-7T= XP_011517007.1:n.953-7T=
XM_017014729.1:c.935-7T= XP_016870218.1:n.935-7T=
NM_054012.4:c.839-7T= MANE Select NP_446464.1:n.839-7T=