Canonical Allele Identifier: CA1129507638

Gene: ASS1

Linked Data

• gnomAD v3: 9-130489260-A-ATTT
• gnomAD v4: 9-130489260-A-ATTT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489261_130489263dup , CM000671.2:g.130489261_130489263dup	GRCh38
NC_000009.11:g.133364648_133364650dup , CM000671.1:g.133364648_133364650dup	GRCh37
NC_000009.10:g.132354469_132354471dup	NCBI36
NG_011542.1:g.49555_49557dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.839-72_839-70dup MANE Select	ENSP00000253004.6:n.839-72_839-70dup
ENST00000352480.9:c.839-72_839-70dup	ENSP00000253004.6:n.839-72_839-70dup
ENST00000372386.6:n.110-72_110-70dup
ENST00000372393.7:c.839-72_839-70dup	ENSP00000361469.2:n.839-72_839-70dup
ENST00000372394.5:c.839-72_839-70dup	ENSP00000361471.1:n.839-72_839-70dup
ENST00000470849.4:n.564-72_564-70dup
ENST00000492400.5:n.348-72_348-70dup
ENST00000493984.6:n.616-72_616-70dup
NM_000050.4:c.839-72_839-70dup	NP_000041.2:n.839-72_839-70dup
NM_054012.3:c.839-72_839-70dup	NP_446464.1:n.839-72_839-70dup
XM_005272200.2:c.839-72_839-70dup	XP_005272257.1:n.839-72_839-70dup
XM_011518705.1:c.953-72_953-70dup	XP_011517007.1:n.953-72_953-70dup
XM_005272200.3:c.839-72_839-70dup	XP_005272257.1:n.839-72_839-70dup
XM_011518705.2:c.953-72_953-70dup	XP_011517007.1:n.953-72_953-70dup
XM_017014729.1:c.935-72_935-70dup	XP_016870218.1:n.935-72_935-70dup
NM_054012.4:c.839-72_839-70dup MANE Select	NP_446464.1:n.839-72_839-70dup