Canonical Allele Identifier: CA1881271273

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130479801G= , CM000671.2:g.130479801G=	GRCh38
NC_000009.11:g.133355188G= , CM000671.1:g.133355188G=	GRCh37
NC_000009.10:g.132345009G=	NCBI36
NG_011542.1:g.40095G=

Transcript Alleles

HGVS	Amino-acid Change
NM_054012.4:c.773+1G= MANE Select	NP_446464.1:n.773+1G=
ENST00000352480.10:c.773+1G= MANE Select	ENSP00000253004.6:n.773+1G=
NM_000050.4:c.773+1G=	NP_000041.2:n.773+1G=
NM_054012.3:c.773+1G=	NP_446464.1:n.773+1G=
ENST00000352480.9:c.773+1G=	ENSP00000253004.6:n.773+1G=
ENST00000372393.7:c.773+1G=	ENSP00000361469.2:n.773+1G=
ENST00000372394.5:c.773+1G=	ENSP00000361471.1:n.773+1G=
ENST00000467695.5:n.483G=
ENST00000470849.4:n.498+1G=
ENST00000492400.5:n.282+1G=
ENST00000493984.6:n.550+1G=
XM_005272200.2:c.773+1G=	XP_005272257.1:n.773+1G=
XM_005272200.3:c.773+1G=	XP_005272257.1:n.773+1G=
XM_011518705.1:c.887+1G=	XP_011517007.1:n.887+1G=
XM_011518705.2:c.887+1G=	XP_011517007.1:n.887+1G=
XM_017014729.1:c.869+1G=	XP_016870218.1:n.869+1G=