Canonical Allele Identifier: CA1881248044
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130455774C= , CM000671.2:g.130455774C= GRCh38
NC_000009.11:g.133331161C= , CM000671.1:g.133331161C= GRCh37
NC_000009.10:g.132320982C= NCBI36
NG_011542.1:g.16068C=

Transcript Alleles

HGVS Amino-acid change
ENST00000352480.10:c.174+1401C= MANE Select ENSP00000253004.6:n.174+1401C=
ENST00000352480.9:c.174+1401C= ENSP00000253004.6:n.174+1401C=
ENST00000372393.7:c.174+1401C= ENSP00000361469.2:n.174+1401C=
ENST00000372394.5:c.174+1401C= ENSP00000361471.1:n.174+1401C=
ENST00000422569.5:c.174+1401C= ENSP00000394212.1:n.174+1401C=
ENST00000443588.1:c.174+1401C= ENSP00000397785.1:n.174+1401C=
NM_000050.4:c.174+1401C= NP_000041.2:n.174+1401C=
NM_054012.3:c.174+1401C= NP_446464.1:n.174+1401C=
XM_005272200.2:c.174+1401C= XP_005272257.1:n.174+1401C=
XM_011518705.1:c.288+1401C= XP_011517007.1:n.288+1401C=
XM_005272200.3:c.174+1401C= XP_005272257.1:n.174+1401C=
XM_011518705.2:c.288+1401C= XP_011517007.1:n.288+1401C=
XM_017014729.1:c.270+1401C= XP_016870218.1:n.270+1401C=
NM_054012.4:c.174+1401C= MANE Select NP_446464.1:n.174+1401C=