Canonical Allele Identifier: CA2692134465
Gene: ASS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130489240_130489241dup , CM000671.2:g.130489240_130489241dup GRCh38
NC_000009.11:g.133364627_133364628dup , CM000671.1:g.133364627_133364628dup GRCh37
NC_000009.10:g.132354448_132354449dup NCBI36
NG_011542.1:g.49534_49535dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.839-93_839-92dup MANE Select ENSP00000253004.6:n.839-93_839-92dup
ENST00000352480.9:c.839-93_839-92dup ENSP00000253004.6:n.839-93_839-92dup
ENST00000372386.6:n.110-93_110-92dup
ENST00000372393.7:c.839-93_839-92dup ENSP00000361469.2:n.839-93_839-92dup
ENST00000372394.5:c.839-93_839-92dup ENSP00000361471.1:n.839-93_839-92dup
ENST00000470849.4:n.564-93_564-92dup
ENST00000492400.5:n.348-93_348-92dup
ENST00000493984.6:n.616-93_616-92dup
NM_000050.4:c.839-93_839-92dup NP_000041.2:n.839-93_839-92dup
NM_054012.3:c.839-93_839-92dup NP_446464.1:n.839-93_839-92dup
XM_005272200.2:c.839-93_839-92dup XP_005272257.1:n.839-93_839-92dup
XM_011518705.1:c.953-93_953-92dup XP_011517007.1:n.953-93_953-92dup
XM_005272200.3:c.839-93_839-92dup XP_005272257.1:n.839-93_839-92dup
XM_011518705.2:c.953-93_953-92dup XP_011517007.1:n.953-93_953-92dup
XM_017014729.1:c.935-93_935-92dup XP_016870218.1:n.935-93_935-92dup
NM_054012.4:c.839-93_839-92dup MANE Select NP_446464.1:n.839-93_839-92dup