Canonical Allele Identifier: CA1881276680
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130489476T= , CM000671.2:g.130489476T= GRCh38
NC_000009.11:g.133364863T= , CM000671.1:g.133364863T= GRCh37
NC_000009.10:g.132354684T= NCBI36
NG_011542.1:g.49770T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.970+12T= MANE Select ENSP00000253004.6:n.970+12T=
ENST00000352480.9:c.970+12T= ENSP00000253004.6:n.970+12T=
ENST00000372386.6:n.241+12T=
ENST00000372393.7:c.970+12T= ENSP00000361469.2:n.970+12T=
ENST00000372394.5:c.970+12T= ENSP00000361471.1:n.970+12T=
NM_000050.4:c.970+12T= NP_000041.2:n.970+12T=
NM_054012.3:c.970+12T= NP_446464.1:n.970+12T=
XM_005272200.2:c.970+12T= XP_005272257.1:n.970+12T=
XM_011518705.1:c.1084+12T= XP_011517007.1:n.1084+12T=
XM_005272200.3:c.970+12T= XP_005272257.1:n.970+12T=
XM_011518705.2:c.1084+12T= XP_011517007.1:n.1084+12T=
XM_017014729.1:c.1066+12T= XP_016870218.1:n.1066+12T=
NM_054012.4:c.970+12T= MANE Select NP_446464.1:n.970+12T=