Canonical Allele Identifier: CA1881275310

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130486442_130486443delinsCT , CM000671.2:g.130486442_130486443delinsCT	GRCh38
NC_000009.11:g.133361829_133361830delinsCT , CM000671.1:g.133361829_133361830delinsCT	GRCh37
NC_000009.10:g.132351650_132351651delinsCT	NCBI36
NG_011542.1:g.46736_46737delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.839-2891_839-2890delinsCT MANE Select	ENSP00000253004.6:n.839-2891_839-2890delinsCT
ENST00000352480.9:c.839-2891_839-2890delinsCT	ENSP00000253004.6:n.839-2891_839-2890delinsCT
ENST00000372386.6:n.110-2891_110-2890delinsCT
ENST00000372393.7:c.839-2891_839-2890delinsCT	ENSP00000361469.2:n.839-2891_839-2890delinsCT
ENST00000372394.5:c.839-2891_839-2890delinsCT	ENSP00000361471.1:n.839-2891_839-2890delinsCT
ENST00000470849.4:n.564-2891_564-2890delinsCT
ENST00000492400.5:n.348-2891_348-2890delinsCT
ENST00000493984.6:n.616-2891_616-2890delinsCT
NM_000050.4:c.839-2891_839-2890delinsCT	NP_000041.2:n.839-2891_839-2890delinsCT
NM_054012.3:c.839-2891_839-2890delinsCT	NP_446464.1:n.839-2891_839-2890delinsCT
XM_005272200.2:c.839-2891_839-2890delinsCT	XP_005272257.1:n.839-2891_839-2890delinsCT
XM_011518705.1:c.953-2891_953-2890delinsCT	XP_011517007.1:n.953-2891_953-2890delinsCT
XM_005272200.3:c.839-2891_839-2890delinsCT	XP_005272257.1:n.839-2891_839-2890delinsCT
XM_011518705.2:c.953-2891_953-2890delinsCT	XP_011517007.1:n.953-2891_953-2890delinsCT
XM_017014729.1:c.935-2891_935-2890delinsCT	XP_016870218.1:n.935-2891_935-2890delinsCT
NM_054012.4:c.839-2891_839-2890delinsCT MANE Select	NP_446464.1:n.839-2891_839-2890delinsCT