Canonical Allele Identifier: CA2579483590
Gene: ASS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130489245_130489248del , CM000671.2:g.130489245_130489248del GRCh38
NC_000009.11:g.133364632_133364635del , CM000671.1:g.133364632_133364635del GRCh37
NC_000009.10:g.132354453_132354456del NCBI36
NG_011542.1:g.49539_49542del

Transcript Alleles

HGVS Amino-acid change
ENST00000352480.10:c.839-88_839-85del MANE Select ENSP00000253004.6:n.839-88_839-85del
ENST00000352480.9:c.839-88_839-85del ENSP00000253004.6:n.839-88_839-85del
ENST00000372386.6:n.110-88_110-85del
ENST00000372393.7:c.839-88_839-85del ENSP00000361469.2:n.839-88_839-85del
ENST00000372394.5:c.839-88_839-85del ENSP00000361471.1:n.839-88_839-85del
ENST00000470849.4:n.564-88_564-85del
ENST00000492400.5:n.348-88_348-85del
ENST00000493984.6:n.616-88_616-85del
NM_000050.4:c.839-88_839-85del NP_000041.2:n.839-88_839-85del
NM_054012.3:c.839-88_839-85del NP_446464.1:n.839-88_839-85del
XM_005272200.2:c.839-88_839-85del XP_005272257.1:n.839-88_839-85del
XM_011518705.1:c.953-88_953-85del XP_011517007.1:n.953-88_953-85del
XM_005272200.3:c.839-88_839-85del XP_005272257.1:n.839-88_839-85del
XM_011518705.2:c.953-88_953-85del XP_011517007.1:n.953-88_953-85del
XM_017014729.1:c.935-88_935-85del XP_016870218.1:n.935-88_935-85del
NM_054012.4:c.839-88_839-85del MANE Select NP_446464.1:n.839-88_839-85del