Canonical Allele Identifier: CA467386101
Community Standard Title: NM_054012.4(ASS1):c.1074G>A (p.Val358=)
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130494970G>A , CM000671.2:g.130494970G>A GRCh38
NC_000009.11:g.133370357G>A , CM000671.1:g.133370357G>A GRCh37
NC_000009.10:g.132360178G>A NCBI36
NG_011542.1:g.55264G>A

Transcript Alleles

HGVS Amino-acid Change
NM_054012.4:c.1074G>A MANE Select NP_446464.1:p.Val358=
ENST00000352480.10:c.1074G>A MANE Select ENSP00000253004.6:p.Val358=
NM_000050.4:c.1074G>A NP_000041.2:p.Val358=
NM_054012.3:c.1074G>A NP_446464.1:p.Val358=
ENST00000352480.9:c.1074G>A ENSP00000253004.6:p.Val358=
ENST00000372386.6:n.345G>A
ENST00000372393.7:c.1074G>A ENSP00000361469.2:p.Val358=
ENST00000372394.5:c.1074G>A ENSP00000361471.1:p.Val358=
XM_005272200.2:c.1074G>A XP_005272257.1:p.Val358=
XM_005272200.3:c.1074G>A XP_005272257.1:p.Val358=
XM_011518705.1:c.1188G>A XP_011517007.1:p.Val396=
XM_011518705.2:c.1188G>A XP_011517007.1:p.Val396=
XM_017014729.1:c.1170G>A XP_016870218.1:p.Val390=
XR_930393.1:n.1060-2713C>T
XR_930393.2:n.1102-2713C>T