Canonical Allele Identifier: CA1881255840
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130470784C= , CM000671.2:g.130470784C= GRCh38
NC_000009.11:g.133346171C= , CM000671.1:g.133346171C= GRCh37
NC_000009.10:g.132335992C= NCBI36
NG_011542.1:g.31078C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.496-50C= MANE Select ENSP00000253004.6:n.496-50C=
ENST00000352480.9:c.496-50C= ENSP00000253004.6:n.496-50C=
ENST00000372393.7:c.496-50C= ENSP00000361469.2:n.496-50C=
ENST00000372394.5:c.496-50C= ENSP00000361471.1:n.496-50C=
ENST00000422569.5:c.496-50C= ENSP00000394212.1:n.496-50C=
ENST00000443588.1:c.439-50C= ENSP00000397785.1:n.439-50C=
ENST00000467695.5:n.205-50C=
ENST00000493984.6:n.327-50C=
NM_000050.4:c.496-50C= NP_000041.2:n.496-50C=
NM_054012.3:c.496-50C= NP_446464.1:n.496-50C=
XM_005272200.2:c.496-50C= XP_005272257.1:n.496-50C=
XM_011518705.1:c.610-50C= XP_011517007.1:n.610-50C=
XM_005272200.3:c.496-50C= XP_005272257.1:n.496-50C=
XM_011518705.2:c.610-50C= XP_011517007.1:n.610-50C=
XM_017014729.1:c.592-50C= XP_016870218.1:n.592-50C=
NM_054012.4:c.496-50C= MANE Select NP_446464.1:n.496-50C=