Canonical Allele Identifier: CA1881276714

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489511T= , CM000671.2:g.130489511T=	GRCh38
NC_000009.11:g.133364898T= , CM000671.1:g.133364898T=	GRCh37
NC_000009.10:g.132354719T=	NCBI36
NG_011542.1:g.49805T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.970+47T= MANE Select	ENSP00000253004.6:n.970+47T=
ENST00000352480.9:c.970+47T=	ENSP00000253004.6:n.970+47T=
ENST00000372386.6:n.241+47T=
ENST00000372393.7:c.970+47T=	ENSP00000361469.2:n.970+47T=
ENST00000372394.5:c.970+47T=	ENSP00000361471.1:n.970+47T=
NM_000050.4:c.970+47T=	NP_000041.2:n.970+47T=
NM_054012.3:c.970+47T=	NP_446464.1:n.970+47T=
XM_005272200.2:c.970+47T=	XP_005272257.1:n.970+47T=
XM_011518705.1:c.1084+47T=	XP_011517007.1:n.1084+47T=
XM_005272200.3:c.970+47T=	XP_005272257.1:n.970+47T=
XM_011518705.2:c.1084+47T=	XP_011517007.1:n.1084+47T=
XM_017014729.1:c.1066+47T=	XP_016870218.1:n.1066+47T=
NM_054012.4:c.970+47T= MANE Select	NP_446464.1:n.970+47T=