Canonical Allele Identifier: CA2579483485

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130471419T>G , CM000671.2:g.130471419T>G	GRCh38
NC_000009.11:g.133346806T>G , CM000671.1:g.133346806T>G	GRCh37
NC_000009.10:g.132336627T>G	NCBI36
NG_011542.1:g.31713T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000352480.10:c.567-66T>G MANE Select	ENSP00000253004.6:n.567-66T>G
ENST00000352480.9:c.567-66T>G	ENSP00000253004.6:n.567-66T>G
ENST00000372393.7:c.567-66T>G	ENSP00000361469.2:n.567-66T>G
ENST00000372394.5:c.567-66T>G	ENSP00000361471.1:n.567-66T>G
ENST00000422569.5:c.567-66T>G	ENSP00000394212.1:n.567-66T>G
ENST00000443588.1:c.510-66T>G	ENSP00000397785.1:n.510-66T>G
ENST00000467695.5:n.276-66T>G
ENST00000493984.6:n.398-66T>G
NM_000050.4:c.567-66T>G	NP_000041.2:n.567-66T>G
NM_054012.3:c.567-66T>G	NP_446464.1:n.567-66T>G
XM_005272200.2:c.567-66T>G	XP_005272257.1:n.567-66T>G
XM_011518705.1:c.681-66T>G	XP_011517007.1:n.681-66T>G
XM_005272200.3:c.567-66T>G	XP_005272257.1:n.567-66T>G
XM_011518705.2:c.681-66T>G	XP_011517007.1:n.681-66T>G
XM_017014729.1:c.663-66T>G	XP_016870218.1:n.663-66T>G
NM_054012.4:c.567-66T>G MANE Select	NP_446464.1:n.567-66T>G