Canonical Allele Identifier: CA2786082784

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489244_130489245insTTTTTT , CM000671.2:g.130489244_130489245insTTTTTT	GRCh38
NC_000009.11:g.133364631_133364632insTTTTTT , CM000671.1:g.133364631_133364632insTTTTTT	GRCh37
NC_000009.10:g.132354452_132354453insTTTTTT	NCBI36
NG_011542.1:g.49538_49539insTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.839-89_839-88insTTTTTT MANE Select	ENSP00000253004.6:n.839-89_839-88insTTTTTT
ENST00000352480.9:c.839-89_839-88insTTTTTT	ENSP00000253004.6:n.839-89_839-88insTTTTTT
ENST00000372386.6:n.110-89_110-88insTTTTTT
ENST00000372393.7:c.839-89_839-88insTTTTTT	ENSP00000361469.2:n.839-89_839-88insTTTTTT
ENST00000372394.5:c.839-89_839-88insTTTTTT	ENSP00000361471.1:n.839-89_839-88insTTTTTT
ENST00000470849.4:n.564-89_564-88insTTTTTT
ENST00000492400.5:n.348-89_348-88insTTTTTT
ENST00000493984.6:n.616-89_616-88insTTTTTT
NM_000050.4:c.839-89_839-88insTTTTTT	NP_000041.2:n.839-89_839-88insTTTTTT
NM_054012.3:c.839-89_839-88insTTTTTT	NP_446464.1:n.839-89_839-88insTTTTTT
XM_005272200.2:c.839-89_839-88insTTTTTT	XP_005272257.1:n.839-89_839-88insTTTTTT
XM_011518705.1:c.953-89_953-88insTTTTTT	XP_011517007.1:n.953-89_953-88insTTTTTT
XM_005272200.3:c.839-89_839-88insTTTTTT	XP_005272257.1:n.839-89_839-88insTTTTTT
XM_011518705.2:c.953-89_953-88insTTTTTT	XP_011517007.1:n.953-89_953-88insTTTTTT
XM_017014729.1:c.935-89_935-88insTTTTTT	XP_016870218.1:n.935-89_935-88insTTTTTT
NM_054012.4:c.839-89_839-88insTTTTTT MANE Select	NP_446464.1:n.839-89_839-88insTTTTTT