Canonical Allele Identifier: CA1129507592
Gene: ASS1 HGNC NCBI

Linked Data

dbSNP Id: rs201358800

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130489244_130489245insTTTTTTTTTT , CM000671.2:g.130489244_130489245insTTTTTTTTTT GRCh38
NC_000009.11:g.133364631_133364632insTTTTTTTTTT , CM000671.1:g.133364631_133364632insTTTTTTTTTT GRCh37
NC_000009.10:g.132354452_132354453insTTTTTTTTTT NCBI36
NG_011542.1:g.49538_49539insTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.839-89_839-88insTTTTTTTTTT MANE Select ENSP00000253004.6:n.839-89_839-88insTTTTTTTTTT
ENST00000352480.9:c.839-89_839-88insTTTTTTTTTT ENSP00000253004.6:n.839-89_839-88insTTTTTTTTTT
ENST00000372386.6:n.110-89_110-88insTTTTTTTTTT
ENST00000372393.7:c.839-89_839-88insTTTTTTTTTT ENSP00000361469.2:n.839-89_839-88insTTTTTTTTTT
ENST00000372394.5:c.839-89_839-88insTTTTTTTTTT ENSP00000361471.1:n.839-89_839-88insTTTTTTTTTT
ENST00000470849.4:n.564-89_564-88insTTTTTTTTTT
ENST00000492400.5:n.348-89_348-88insTTTTTTTTTT
ENST00000493984.6:n.616-89_616-88insTTTTTTTTTT
NM_000050.4:c.839-89_839-88insTTTTTTTTTT NP_000041.2:n.839-89_839-88insTTTTTTTTTT
NM_054012.3:c.839-89_839-88insTTTTTTTTTT NP_446464.1:n.839-89_839-88insTTTTTTTTTT
XM_005272200.2:c.839-89_839-88insTTTTTTTTTT XP_005272257.1:n.839-89_839-88insTTTTTTTTTT
XM_011518705.1:c.953-89_953-88insTTTTTTTTTT XP_011517007.1:n.953-89_953-88insTTTTTTTTTT
XM_005272200.3:c.839-89_839-88insTTTTTTTTTT XP_005272257.1:n.839-89_839-88insTTTTTTTTTT
XM_011518705.2:c.953-89_953-88insTTTTTTTTTT XP_011517007.1:n.953-89_953-88insTTTTTTTTTT
XM_017014729.1:c.935-89_935-88insTTTTTTTTTT XP_016870218.1:n.935-89_935-88insTTTTTTTTTT
NM_054012.4:c.839-89_839-88insTTTTTTTTTT MANE Select NP_446464.1:n.839-89_839-88insTTTTTTTTTT