Canonical Allele Identifier: CA1881271782
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130480324G= , CM000671.2:g.130480324G= GRCh38
NC_000009.11:g.133355711G= , CM000671.1:g.133355711G= GRCh37
NC_000009.10:g.132345532G= NCBI36
NG_011542.1:g.40618G=

Transcript Alleles

HGVS Amino-acid change
ENST00000352480.10:c.774-61G= MANE Select ENSP00000253004.6:n.774-61G=
ENST00000352480.9:c.774-61G= ENSP00000253004.6:n.774-61G=
ENST00000372386.6:n.45-61G=
ENST00000372393.7:c.774-61G= ENSP00000361469.2:n.774-61G=
ENST00000372394.5:c.774-61G= ENSP00000361471.1:n.774-61G=
ENST00000470849.4:n.499-61G=
ENST00000492400.5:n.283-61G=
ENST00000493984.6:n.551-61G=
NM_000050.4:c.774-61G= NP_000041.2:n.774-61G=
NM_054012.3:c.774-61G= NP_446464.1:n.774-61G=
XM_005272200.2:c.774-61G= XP_005272257.1:n.774-61G=
XM_011518705.1:c.888-61G= XP_011517007.1:n.888-61G=
XM_005272200.3:c.774-61G= XP_005272257.1:n.774-61G=
XM_011518705.2:c.888-61G= XP_011517007.1:n.888-61G=
XM_017014729.1:c.870-61G= XP_016870218.1:n.870-61G=
NM_054012.4:c.774-61G= MANE Select NP_446464.1:n.774-61G=