Canonical Allele Identifier: CA1881244192
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130452031_130452033delinsCAG , CM000671.2:g.130452031_130452033delinsCAG GRCh38
NC_000009.11:g.133327418_133327420delinsCAG , CM000671.1:g.133327418_133327420delinsCAG GRCh37
NC_000009.10:g.132317239_132317241delinsCAG NCBI36
NG_011542.1:g.12325_12327delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.-5-193_-5-191delinsCAG MANE Select ENSP00000253004.6:n.-5-193_-5-191delinsCAG
ENST00000352480.9:c.-5-193_-5-191delinsCAG ENSP00000253004.6:n.-5-193_-5-191delinsCAG
ENST00000372393.7:c.-5-193_-5-191delinsCAG ENSP00000361469.2:n.-5-193_-5-191delinsCAG
ENST00000372394.5:c.-18_-16delinsCAG ENSP00000361471.1:n.-18_-16delinsCAG
ENST00000422569.5:c.-5-193_-5-191delinsCAG ENSP00000394212.1:n.-5-193_-5-191delinsCAG
NM_000050.4:c.-5-193_-5-191delinsCAG NP_000041.2:n.-5-193_-5-191delinsCAG
NM_054012.3:c.-5-193_-5-191delinsCAG NP_446464.1:n.-5-193_-5-191delinsCAG
XM_005272200.2:c.-5-193_-5-191delinsCAG XP_005272257.1:n.-5-193_-5-191delinsCAG
XM_011518705.1:c.110-193_110-191delinsCAG XP_011517007.1:n.110-193_110-191delinsCAG
XM_005272200.3:c.-5-193_-5-191delinsCAG XP_005272257.1:n.-5-193_-5-191delinsCAG
XM_011518705.2:c.110-193_110-191delinsCAG XP_011517007.1:n.110-193_110-191delinsCAG
XM_017014729.1:c.92-193_92-191delinsCAG XP_016870218.1:n.92-193_92-191delinsCAG
NM_054012.4:c.-5-193_-5-191delinsCAG MANE Select NP_446464.1:n.-5-193_-5-191delinsCAG