Canonical Allele Identifier: CA2579483589
Gene: ASS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130489242_130489245del , CM000671.2:g.130489242_130489245del GRCh38
NC_000009.11:g.133364629_133364632del , CM000671.1:g.133364629_133364632del GRCh37
NC_000009.10:g.132354450_132354453del NCBI36
NG_011542.1:g.49536_49539del

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.839-91_839-88del MANE Select ENSP00000253004.6:n.839-91_839-88del
ENST00000352480.9:c.839-91_839-88del ENSP00000253004.6:n.839-91_839-88del
ENST00000372386.6:n.110-91_110-88del
ENST00000372393.7:c.839-91_839-88del ENSP00000361469.2:n.839-91_839-88del
ENST00000372394.5:c.839-91_839-88del ENSP00000361471.1:n.839-91_839-88del
ENST00000470849.4:n.564-91_564-88del
ENST00000492400.5:n.348-91_348-88del
ENST00000493984.6:n.616-91_616-88del
NM_000050.4:c.839-91_839-88del NP_000041.2:n.839-91_839-88del
NM_054012.3:c.839-91_839-88del NP_446464.1:n.839-91_839-88del
XM_005272200.2:c.839-91_839-88del XP_005272257.1:n.839-91_839-88del
XM_011518705.1:c.953-91_953-88del XP_011517007.1:n.953-91_953-88del
XM_005272200.3:c.839-91_839-88del XP_005272257.1:n.839-91_839-88del
XM_011518705.2:c.953-91_953-88del XP_011517007.1:n.953-91_953-88del
XM_017014729.1:c.935-91_935-88del XP_016870218.1:n.935-91_935-88del
NM_054012.4:c.839-91_839-88del MANE Select NP_446464.1:n.839-91_839-88del