Canonical Allele Identifier: CA1881248011
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130455746G= , CM000671.2:g.130455746G= GRCh38
NC_000009.11:g.133331133G= , CM000671.1:g.133331133G= GRCh37
NC_000009.10:g.132320954G= NCBI36
NG_011542.1:g.16040G=

Transcript Alleles

HGVS Amino-acid change
ENST00000352480.10:c.174+1373G= MANE Select ENSP00000253004.6:n.174+1373G=
ENST00000352480.9:c.174+1373G= ENSP00000253004.6:n.174+1373G=
ENST00000372393.7:c.174+1373G= ENSP00000361469.2:n.174+1373G=
ENST00000372394.5:c.174+1373G= ENSP00000361471.1:n.174+1373G=
ENST00000422569.5:c.174+1373G= ENSP00000394212.1:n.174+1373G=
ENST00000443588.1:c.174+1373G= ENSP00000397785.1:n.174+1373G=
NM_000050.4:c.174+1373G= NP_000041.2:n.174+1373G=
NM_054012.3:c.174+1373G= NP_446464.1:n.174+1373G=
XM_005272200.2:c.174+1373G= XP_005272257.1:n.174+1373G=
XM_011518705.1:c.288+1373G= XP_011517007.1:n.288+1373G=
XM_005272200.3:c.174+1373G= XP_005272257.1:n.174+1373G=
XM_011518705.2:c.288+1373G= XP_011517007.1:n.288+1373G=
XM_017014729.1:c.270+1373G= XP_016870218.1:n.270+1373G=
NM_054012.4:c.174+1373G= MANE Select NP_446464.1:n.174+1373G=