Canonical Allele Identifier: CA2692134532
Gene: ASS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130489247_130489248insATTTT , CM000671.2:g.130489247_130489248insATTTT GRCh38
NC_000009.11:g.133364634_133364635insATTTT , CM000671.1:g.133364634_133364635insATTTT GRCh37
NC_000009.10:g.132354455_132354456insATTTT NCBI36
NG_011542.1:g.49541_49542insATTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.839-86_839-85insATTTT MANE Select ENSP00000253004.6:n.839-86_839-85insATTTT
ENST00000352480.9:c.839-86_839-85insATTTT ENSP00000253004.6:n.839-86_839-85insATTTT
ENST00000372386.6:n.110-86_110-85insATTTT
ENST00000372393.7:c.839-86_839-85insATTTT ENSP00000361469.2:n.839-86_839-85insATTTT
ENST00000372394.5:c.839-86_839-85insATTTT ENSP00000361471.1:n.839-86_839-85insATTTT
ENST00000470849.4:n.564-86_564-85insATTTT
ENST00000492400.5:n.348-86_348-85insATTTT
ENST00000493984.6:n.616-86_616-85insATTTT
NM_000050.4:c.839-86_839-85insATTTT NP_000041.2:n.839-86_839-85insATTTT
NM_054012.3:c.839-86_839-85insATTTT NP_446464.1:n.839-86_839-85insATTTT
XM_005272200.2:c.839-86_839-85insATTTT XP_005272257.1:n.839-86_839-85insATTTT
XM_011518705.1:c.953-86_953-85insATTTT XP_011517007.1:n.953-86_953-85insATTTT
XM_005272200.3:c.839-86_839-85insATTTT XP_005272257.1:n.839-86_839-85insATTTT
XM_011518705.2:c.953-86_953-85insATTTT XP_011517007.1:n.953-86_953-85insATTTT
XM_017014729.1:c.935-86_935-85insATTTT XP_016870218.1:n.935-86_935-85insATTTT
NM_054012.4:c.839-86_839-85insATTTT MANE Select NP_446464.1:n.839-86_839-85insATTTT