Canonical Allele Identifier: CA1881249933
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130458403G= , CM000671.2:g.130458403G= GRCh38
NC_000009.11:g.133333790G= , CM000671.1:g.133333790G= GRCh37
NC_000009.10:g.132323611G= NCBI36
NG_011542.1:g.18697G=

Transcript Alleles

HGVS Amino-acid change
ENST00000352480.10:c.177G= MANE Select ENSP00000253004.6:p.Val59=
ENST00000352480.9:c.177G= ENSP00000253004.6:p.Val59=
ENST00000372393.7:c.177G= ENSP00000361469.2:p.Val59=
ENST00000372394.5:c.177G= ENSP00000361471.1:p.Val59=
ENST00000422569.5:c.177G= ENSP00000394212.1:p.Val59=
ENST00000443588.1:c.177G= ENSP00000397785.1:p.Val59=
NM_000050.4:c.177G= NP_000041.2:p.Val59=
NM_054012.3:c.177G= NP_446464.1:p.Val59=
XM_005272200.2:c.177G= XP_005272257.1:p.Val59=
XM_011518705.1:c.291G= XP_011517007.1:p.Val97=
XM_005272200.3:c.177G= XP_005272257.1:p.Val59=
XM_011518705.2:c.291G= XP_011517007.1:p.Val97=
XM_017014729.1:c.273G= XP_016870218.1:p.Val91=
NM_054012.4:c.177G= MANE Select NP_446464.1:p.Val59=