Canonical Allele Identifier: CA1881276569
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130489232_130489235delinsCATT , CM000671.2:g.130489232_130489235delinsCATT GRCh38
NC_000009.11:g.133364619_133364622delinsCATT , CM000671.1:g.133364619_133364622delinsCATT GRCh37
NC_000009.10:g.132354440_132354443delinsCATT NCBI36
NG_011542.1:g.49526_49529delinsCATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.839-101_839-98delinsCATT MANE Select ENSP00000253004.6:n.839-101_839-98delinsCATT
ENST00000352480.9:c.839-101_839-98delinsCATT ENSP00000253004.6:n.839-101_839-98delinsCATT
ENST00000372386.6:n.110-101_110-98delinsCATT
ENST00000372393.7:c.839-101_839-98delinsCATT ENSP00000361469.2:n.839-101_839-98delinsCATT
ENST00000372394.5:c.839-101_839-98delinsCATT ENSP00000361471.1:n.839-101_839-98delinsCATT
ENST00000470849.4:n.564-101_564-98delinsCATT
ENST00000492400.5:n.348-101_348-98delinsCATT
ENST00000493984.6:n.616-101_616-98delinsCATT
NM_000050.4:c.839-101_839-98delinsCATT NP_000041.2:n.839-101_839-98delinsCATT
NM_054012.3:c.839-101_839-98delinsCATT NP_446464.1:n.839-101_839-98delinsCATT
XM_005272200.2:c.839-101_839-98delinsCATT XP_005272257.1:n.839-101_839-98delinsCATT
XM_011518705.1:c.953-101_953-98delinsCATT XP_011517007.1:n.953-101_953-98delinsCATT
XM_005272200.3:c.839-101_839-98delinsCATT XP_005272257.1:n.839-101_839-98delinsCATT
XM_011518705.2:c.953-101_953-98delinsCATT XP_011517007.1:n.953-101_953-98delinsCATT
XM_017014729.1:c.935-101_935-98delinsCATT XP_016870218.1:n.935-101_935-98delinsCATT
NM_054012.4:c.839-101_839-98delinsCATT MANE Select NP_446464.1:n.839-101_839-98delinsCATT