Canonical Allele Identifier: CA375223665
Gene: ASS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130452330T>G , CM000671.2:g.130452330T>G GRCh38
NC_000009.11:g.133327717T>G , CM000671.1:g.133327717T>G GRCh37
NC_000009.10:g.132317538T>G NCBI36
NG_011542.1:g.12624T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.102T>G MANE Select ENSP00000253004.6:p.Tyr34Ter
ENST00000352480.9:c.102T>G ENSP00000253004.6:p.Tyr34Ter
ENST00000372393.7:c.102T>G ENSP00000361469.2:p.Tyr34Ter
ENST00000372394.5:c.102T>G ENSP00000361471.1:p.Tyr34Ter
ENST00000422569.5:c.102T>G ENSP00000394212.1:p.Tyr34Ter
ENST00000443588.1:c.102T>G ENSP00000397785.1:p.Tyr34Ter
NM_000050.4:c.102T>G NP_000041.2:p.Tyr34Ter
NM_054012.3:c.102T>G NP_446464.1:p.Tyr34Ter
XM_005272200.2:c.102T>G XP_005272257.1:p.Tyr34Ter
XM_011518705.1:c.216T>G XP_011517007.1:p.Tyr72Ter
XM_005272200.3:c.102T>G XP_005272257.1:p.Tyr34Ter
XM_011518705.2:c.216T>G XP_011517007.1:p.Tyr72Ter
XM_017014729.1:c.198T>G XP_016870218.1:p.Tyr66Ter
NM_054012.4:c.102T>G MANE Select NP_446464.1:p.Tyr34Ter