Canonical Allele Identifier: CA1881276613
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130489335A= , CM000671.2:g.130489335A= GRCh38
NC_000009.11:g.133364722A= , CM000671.1:g.133364722A= GRCh37
NC_000009.10:g.132354543A= NCBI36
NG_011542.1:g.49629A=

Transcript Alleles

HGVS Amino-acid change
ENST00000352480.10:c.841A= MANE Select ENSP00000253004.6:p.Ile281=
ENST00000352480.9:c.841A= ENSP00000253004.6:p.Ile281=
ENST00000372386.6:n.112A=
ENST00000372393.7:c.841A= ENSP00000361469.2:p.Ile281=
ENST00000372394.5:c.841A= ENSP00000361471.1:p.Ile281=
ENST00000470849.4:n.566A=
ENST00000492400.5:n.350A=
ENST00000493984.6:n.618A=
NM_000050.4:c.841A= NP_000041.2:p.Ile281=
NM_054012.3:c.841A= NP_446464.1:p.Ile281=
XM_005272200.2:c.841A= XP_005272257.1:p.Ile281=
XM_011518705.1:c.955A= XP_011517007.1:p.Ile319=
XM_005272200.3:c.841A= XP_005272257.1:p.Ile281=
XM_011518705.2:c.955A= XP_011517007.1:p.Ile319=
XM_017014729.1:c.937A= XP_016870218.1:p.Ile313=
NM_054012.4:c.841A= MANE Select NP_446464.1:p.Ile281=