Canonical Allele Identifier: CA2692119326
Gene: ASS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130452229_130452230del , CM000671.2:g.130452229_130452230del GRCh38
NC_000009.11:g.133327616_133327617del , CM000671.1:g.133327616_133327617del GRCh37
NC_000009.10:g.132317437_132317438del NCBI36
NG_011542.1:g.12523_12524del

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.1_2del MANE Select ENSP00000253004.6:p.Met1ValfsTer29
ENST00000352480.9:c.1_2del ENSP00000253004.6:p.Met1ValfsTer29
ENST00000372393.7:c.1_2del ENSP00000361469.2:p.Met1ValfsTer29
ENST00000372394.5:c.1_2del ENSP00000361471.1:p.Met1ValfsTer29
ENST00000422569.5:c.1_2del ENSP00000394212.1:p.Met1ValfsTer29
ENST00000443588.1:c.1_2del ENSP00000397785.1:p.Met1ValfsTer29
NM_000050.4:c.1_2del NP_000041.2:p.Met1ValfsTer29
NM_054012.3:c.1_2del NP_446464.1:p.Met1ValfsTer29
XM_005272200.2:c.1_2del XP_005272257.1:p.Met1ValfsTer29
XM_011518705.1:c.115_116del XP_011517007.1:p.Met39ValfsTer29
XM_005272200.3:c.1_2del XP_005272257.1:p.Met1ValfsTer29
XM_011518705.2:c.115_116del XP_011517007.1:p.Met39ValfsTer29
XM_017014729.1:c.97_98del XP_016870218.1:p.Met33ValfsTer29
NM_054012.4:c.1_2del MANE Select NP_446464.1:p.Met1ValfsTer29