Canonical Allele Identifier: CA2579483609
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130489514del , CM000671.2:g.130489514del GRCh38
NC_000009.11:g.133364901del , CM000671.1:g.133364901del GRCh37
NC_000009.10:g.132354722del NCBI36
NG_011542.1:g.49808del

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.970+50del MANE Select ENSP00000253004.6:n.970+50del
ENST00000352480.9:c.970+50del ENSP00000253004.6:n.970+50del
ENST00000372386.6:n.241+50del
ENST00000372393.7:c.970+50del ENSP00000361469.2:n.970+50del
ENST00000372394.5:c.970+50del ENSP00000361471.1:n.970+50del
NM_000050.4:c.970+50del NP_000041.2:n.970+50del
NM_054012.3:c.970+50del NP_446464.1:n.970+50del
XM_005272200.2:c.970+50del XP_005272257.1:n.970+50del
XM_011518705.1:c.1084+50del XP_011517007.1:n.1084+50del
XM_005272200.3:c.970+50del XP_005272257.1:n.970+50del
XM_011518705.2:c.1084+50del XP_011517007.1:n.1084+50del
XM_017014729.1:c.1066+50del XP_016870218.1:n.1066+50del
NM_054012.4:c.970+50del MANE Select NP_446464.1:n.970+50del