Canonical Allele Identifier: CA2843284112
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130452192G>T , CM000671.2:g.130452192G>T GRCh38
NC_000009.11:g.133327579G>T , CM000671.1:g.133327579G>T GRCh37
NC_000009.10:g.132317400G>T NCBI36
NG_011542.1:g.12486G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.-5-32G>T MANE Select ENSP00000253004.6:n.-5-32G>T
ENST00000352480.9:c.-5-32G>T ENSP00000253004.6:n.-5-32G>T
ENST00000372393.7:c.-5-32G>T ENSP00000361469.2:n.-5-32G>T
ENST00000372394.5:c.-5-32G>T ENSP00000361471.1:n.-5-32G>T
ENST00000422569.5:c.-5-32G>T ENSP00000394212.1:n.-5-32G>T
NM_000050.4:c.-5-32G>T NP_000041.2:n.-5-32G>T
NM_054012.3:c.-5-32G>T NP_446464.1:n.-5-32G>T
XM_005272200.2:c.-5-32G>T XP_005272257.1:n.-5-32G>T
XM_011518705.1:c.110-32G>T XP_011517007.1:n.110-32G>T
XM_005272200.3:c.-5-32G>T XP_005272257.1:n.-5-32G>T
XM_011518705.2:c.110-32G>T XP_011517007.1:n.110-32G>T
XM_017014729.1:c.92-32G>T XP_016870218.1:n.92-32G>T
NM_054012.4:c.-5-32G>T MANE Select NP_446464.1:n.-5-32G>T