Canonical Allele Identifier: CA2579483601
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130489299_130489300del , CM000671.2:g.130489299_130489300del GRCh38
NC_000009.11:g.133364686_133364687del , CM000671.1:g.133364686_133364687del GRCh37
NC_000009.10:g.132354507_132354508del NCBI36
NG_011542.1:g.49593_49594del

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.839-34_839-33del MANE Select ENSP00000253004.6:n.839-34_839-33del
ENST00000352480.9:c.839-34_839-33del ENSP00000253004.6:n.839-34_839-33del
ENST00000372386.6:n.110-34_110-33del
ENST00000372393.7:c.839-34_839-33del ENSP00000361469.2:n.839-34_839-33del
ENST00000372394.5:c.839-34_839-33del ENSP00000361471.1:n.839-34_839-33del
ENST00000470849.4:n.564-34_564-33del
ENST00000492400.5:n.348-34_348-33del
ENST00000493984.6:n.616-34_616-33del
NM_000050.4:c.839-34_839-33del NP_000041.2:n.839-34_839-33del
NM_054012.3:c.839-34_839-33del NP_446464.1:n.839-34_839-33del
XM_005272200.2:c.839-34_839-33del XP_005272257.1:n.839-34_839-33del
XM_011518705.1:c.953-34_953-33del XP_011517007.1:n.953-34_953-33del
XM_005272200.3:c.839-34_839-33del XP_005272257.1:n.839-34_839-33del
XM_011518705.2:c.953-34_953-33del XP_011517007.1:n.953-34_953-33del
XM_017014729.1:c.935-34_935-33del XP_016870218.1:n.935-34_935-33del
NM_054012.4:c.839-34_839-33del MANE Select NP_446464.1:n.839-34_839-33del