Canonical Allele Identifier: CA1881256251

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130471492G= , CM000671.2:g.130471492G=	GRCh38
NC_000009.11:g.133346879G= , CM000671.1:g.133346879G=	GRCh37
NC_000009.10:g.132336700G=	NCBI36
NG_011542.1:g.31786G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000352480.10:c.574G= MANE Select	ENSP00000253004.6:p.Ala192=
ENST00000352480.9:c.574G=	ENSP00000253004.6:p.Ala192=
ENST00000372393.7:c.574G=	ENSP00000361469.2:p.Ala192=
ENST00000372394.5:c.574G=	ENSP00000361471.1:p.Ala192=
ENST00000422569.5:c.574G=	ENSP00000394212.1:p.Ala192=
ENST00000443588.1:c.517G=	ENSP00000397785.1:p.Ala173=
ENST00000467695.5:n.283G=
ENST00000493984.6:n.405G=
NM_000050.4:c.574G=	NP_000041.2:p.Ala192=
NM_054012.3:c.574G=	NP_446464.1:p.Ala192=
XM_005272200.2:c.574G=	XP_005272257.1:p.Ala192=
XM_011518705.1:c.688G=	XP_011517007.1:p.Ala230=
XM_005272200.3:c.574G=	XP_005272257.1:p.Ala192=
XM_011518705.2:c.688G=	XP_011517007.1:p.Ala230=
XM_017014729.1:c.670G=	XP_016870218.1:p.Ala224=
NM_054012.4:c.574G= MANE Select	NP_446464.1:p.Ala192=