Canonical Allele Identifier: CA375230611
Gene: ASS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130489407G>A , CM000671.2:g.130489407G>A GRCh38
NC_000009.11:g.133364794G>A , CM000671.1:g.133364794G>A GRCh37
NC_000009.10:g.132354615G>A NCBI36
NG_011542.1:g.49701G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.913G>A MANE Select ENSP00000253004.6:p.Glu305Lys
ENST00000352480.9:c.913G>A ENSP00000253004.6:p.Glu305Lys
ENST00000372386.6:n.184G>A
ENST00000372393.7:c.913G>A ENSP00000361469.2:p.Glu305Lys
ENST00000372394.5:c.913G>A ENSP00000361471.1:p.Glu305Lys
ENST00000470849.4:n.638G>A
ENST00000492400.5:n.422G>A
NM_000050.4:c.913G>A NP_000041.2:p.Glu305Lys
NM_054012.3:c.913G>A NP_446464.1:p.Glu305Lys
XM_005272200.2:c.913G>A XP_005272257.1:p.Glu305Lys
XM_011518705.1:c.1027G>A XP_011517007.1:p.Glu343Lys
XM_005272200.3:c.913G>A XP_005272257.1:p.Glu305Lys
XM_011518705.2:c.1027G>A XP_011517007.1:p.Glu343Lys
XM_017014729.1:c.1009G>A XP_016870218.1:p.Glu337Lys
NM_054012.4:c.913G>A MANE Select NP_446464.1:p.Glu305Lys