Canonical Allele Identifier: CA2692134438

Gene: ASS1

Linked Data

• gnomAD v4: 9-130489232-C-CATTATT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489242_130489247dup , CM000671.2:g.130489242_130489247dup	GRCh38
NC_000009.11:g.133364629_133364634dup , CM000671.1:g.133364629_133364634dup	GRCh37
NC_000009.10:g.132354450_132354455dup	NCBI36
NG_011542.1:g.49536_49541dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000352480.10:c.839-91_839-86dup MANE Select	ENSP00000253004.6:n.839-91_839-86dup
ENST00000352480.9:c.839-91_839-86dup	ENSP00000253004.6:n.839-91_839-86dup
ENST00000372386.6:n.110-91_110-86dup
ENST00000372393.7:c.839-91_839-86dup	ENSP00000361469.2:n.839-91_839-86dup
ENST00000372394.5:c.839-91_839-86dup	ENSP00000361471.1:n.839-91_839-86dup
ENST00000470849.4:n.564-91_564-86dup
ENST00000492400.5:n.348-91_348-86dup
ENST00000493984.6:n.616-91_616-86dup
NM_000050.4:c.839-91_839-86dup	NP_000041.2:n.839-91_839-86dup
NM_054012.3:c.839-91_839-86dup	NP_446464.1:n.839-91_839-86dup
XM_005272200.2:c.839-91_839-86dup	XP_005272257.1:n.839-91_839-86dup
XM_011518705.1:c.953-91_953-86dup	XP_011517007.1:n.953-91_953-86dup
XM_005272200.3:c.839-91_839-86dup	XP_005272257.1:n.839-91_839-86dup
XM_011518705.2:c.953-91_953-86dup	XP_011517007.1:n.953-91_953-86dup
XM_017014729.1:c.935-91_935-86dup	XP_016870218.1:n.935-91_935-86dup
NM_054012.4:c.839-91_839-86dup MANE Select	NP_446464.1:n.839-91_839-86dup