Canonical Allele Identifier: CA1881276614
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130489340C= , CM000671.2:g.130489340C= GRCh38
NC_000009.11:g.133364727C= , CM000671.1:g.133364727C= GRCh37
NC_000009.10:g.132354548C= NCBI36
NG_011542.1:g.49634C=

Transcript Alleles

HGVS Amino-acid change
ENST00000352480.10:c.846C= MANE Select ENSP00000253004.6:p.Tyr282=
ENST00000352480.9:c.846C= ENSP00000253004.6:p.Tyr282=
ENST00000372386.6:n.117C=
ENST00000372393.7:c.846C= ENSP00000361469.2:p.Tyr282=
ENST00000372394.5:c.846C= ENSP00000361471.1:p.Tyr282=
ENST00000470849.4:n.571C=
ENST00000492400.5:n.355C=
ENST00000493984.6:n.623C=
NM_000050.4:c.846C= NP_000041.2:p.Tyr282=
NM_054012.3:c.846C= NP_446464.1:p.Tyr282=
XM_005272200.2:c.846C= XP_005272257.1:p.Tyr282=
XM_011518705.1:c.960C= XP_011517007.1:p.Tyr320=
XM_005272200.3:c.846C= XP_005272257.1:p.Tyr282=
XM_011518705.2:c.960C= XP_011517007.1:p.Tyr320=
XM_017014729.1:c.942C= XP_016870218.1:p.Tyr314=
NM_054012.4:c.846C= MANE Select NP_446464.1:p.Tyr282=