Canonical Allele Identifier: CA1881275314

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130486452_130486454delinsCCT , CM000671.2:g.130486452_130486454delinsCCT	GRCh38
NC_000009.11:g.133361839_133361841delinsCCT , CM000671.1:g.133361839_133361841delinsCCT	GRCh37
NC_000009.10:g.132351660_132351662delinsCCT	NCBI36
NG_011542.1:g.46746_46748delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.839-2881_839-2879delinsCCT MANE Select	ENSP00000253004.6:n.839-2881_839-2879delinsCCT
ENST00000352480.9:c.839-2881_839-2879delinsCCT	ENSP00000253004.6:n.839-2881_839-2879delinsCCT
ENST00000372386.6:n.110-2881_110-2879delinsCCT
ENST00000372393.7:c.839-2881_839-2879delinsCCT	ENSP00000361469.2:n.839-2881_839-2879delinsCCT
ENST00000372394.5:c.839-2881_839-2879delinsCCT	ENSP00000361471.1:n.839-2881_839-2879delinsCCT
ENST00000470849.4:n.564-2881_564-2879delinsCCT
ENST00000492400.5:n.348-2881_348-2879delinsCCT
ENST00000493984.6:n.616-2881_616-2879delinsCCT
NM_000050.4:c.839-2881_839-2879delinsCCT	NP_000041.2:n.839-2881_839-2879delinsCCT
NM_054012.3:c.839-2881_839-2879delinsCCT	NP_446464.1:n.839-2881_839-2879delinsCCT
XM_005272200.2:c.839-2881_839-2879delinsCCT	XP_005272257.1:n.839-2881_839-2879delinsCCT
XM_011518705.1:c.953-2881_953-2879delinsCCT	XP_011517007.1:n.953-2881_953-2879delinsCCT
XM_005272200.3:c.839-2881_839-2879delinsCCT	XP_005272257.1:n.839-2881_839-2879delinsCCT
XM_011518705.2:c.953-2881_953-2879delinsCCT	XP_011517007.1:n.953-2881_953-2879delinsCCT
XM_017014729.1:c.935-2881_935-2879delinsCCT	XP_016870218.1:n.935-2881_935-2879delinsCCT
NM_054012.4:c.839-2881_839-2879delinsCCT MANE Select	NP_446464.1:n.839-2881_839-2879delinsCCT