Canonical Allele Identifier: CA1129507623
Gene: ASS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130489255_130489256del , CM000671.2:g.130489255_130489256del GRCh38
NC_000009.11:g.133364642_133364643del , CM000671.1:g.133364642_133364643del GRCh37
NC_000009.10:g.132354463_132354464del NCBI36
NG_011542.1:g.49549_49550del

Transcript Alleles

HGVS Amino-acid change
ENST00000352480.10:c.839-78_839-77del MANE Select ENSP00000253004.6:n.839-78_839-77del
ENST00000352480.9:c.839-78_839-77del ENSP00000253004.6:n.839-78_839-77del
ENST00000372386.6:n.110-78_110-77del
ENST00000372393.7:c.839-78_839-77del ENSP00000361469.2:n.839-78_839-77del
ENST00000372394.5:c.839-78_839-77del ENSP00000361471.1:n.839-78_839-77del
ENST00000470849.4:n.564-78_564-77del
ENST00000492400.5:n.348-78_348-77del
ENST00000493984.6:n.616-78_616-77del
NM_000050.4:c.839-78_839-77del NP_000041.2:n.839-78_839-77del
NM_054012.3:c.839-78_839-77del NP_446464.1:n.839-78_839-77del
XM_005272200.2:c.839-78_839-77del XP_005272257.1:n.839-78_839-77del
XM_011518705.1:c.953-78_953-77del XP_011517007.1:n.953-78_953-77del
XM_005272200.3:c.839-78_839-77del XP_005272257.1:n.839-78_839-77del
XM_011518705.2:c.953-78_953-77del XP_011517007.1:n.953-78_953-77del
XM_017014729.1:c.935-78_935-77del XP_016870218.1:n.935-78_935-77del
NM_054012.4:c.839-78_839-77del MANE Select NP_446464.1:n.839-78_839-77del