Canonical Allele Identifier: CA2579483303
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130452182del , CM000671.2:g.130452182del GRCh38
NC_000009.11:g.133327569del , CM000671.1:g.133327569del GRCh37
NC_000009.10:g.132317390del NCBI36
NG_011542.1:g.12476del

Transcript Alleles

HGVS Amino-acid change
ENST00000352480.10:c.-5-42del MANE Select ENSP00000253004.6:n.-5-42del
ENST00000352480.9:c.-5-42del ENSP00000253004.6:n.-5-42del
ENST00000372393.7:c.-5-42del ENSP00000361469.2:n.-5-42del
ENST00000372394.5:c.-5-42del ENSP00000361471.1:n.-5-42del
ENST00000422569.5:c.-5-42del ENSP00000394212.1:n.-5-42del
NM_000050.4:c.-5-42del NP_000041.2:n.-5-42del
NM_054012.3:c.-5-42del NP_446464.1:n.-5-42del
XM_005272200.2:c.-5-42del XP_005272257.1:n.-5-42del
XM_011518705.1:c.110-42del XP_011517007.1:n.110-42del
XM_005272200.3:c.-5-42del XP_005272257.1:n.-5-42del
XM_011518705.2:c.110-42del XP_011517007.1:n.110-42del
XM_017014729.1:c.92-42del XP_016870218.1:n.92-42del
NM_054012.4:c.-5-42del MANE Select NP_446464.1:n.-5-42del