Canonical Allele Identifier: CA5283130
Community Standard Title: NM_054012.4(ASS1):c.39C>T (p.Gly13=)
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130452267C>T , CM000671.2:g.130452267C>T GRCh38
NC_000009.11:g.133327654C>T , CM000671.1:g.133327654C>T GRCh37
NC_000009.10:g.132317475C>T NCBI36
NG_011542.1:g.12561C>T

Transcript Alleles

HGVS Amino-acid Change
NM_054012.4:c.39C>T MANE Select NP_446464.1:p.Gly13=
ENST00000352480.10:c.39C>T MANE Select ENSP00000253004.6:p.Gly13=
NM_000050.4:c.39C>T NP_000041.2:p.Gly13=
NM_054012.3:c.39C>T NP_446464.1:p.Gly13=
ENST00000352480.9:c.39C>T ENSP00000253004.6:p.Gly13=
ENST00000372393.7:c.39C>T ENSP00000361469.2:p.Gly13=
ENST00000372394.5:c.39C>T ENSP00000361471.1:p.Gly13=
ENST00000422569.5:c.39C>T ENSP00000394212.1:p.Gly13=
ENST00000443588.1:c.39C>T ENSP00000397785.1:p.Gly13=
XM_005272200.2:c.39C>T XP_005272257.1:p.Gly13=
XM_005272200.3:c.39C>T XP_005272257.1:p.Gly13=
XM_011518705.1:c.153C>T XP_011517007.1:p.Gly51=
XM_011518705.2:c.153C>T XP_011517007.1:p.Gly51=
XM_017014729.1:c.135C>T XP_016870218.1:p.Gly45=