Canonical Allele Identifier: CA2692134620

Gene: ASS1

Linked Data

• gnomAD v4: 9-130489263-TGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489264_130489265del , CM000671.2:g.130489264_130489265del	GRCh38
NC_000009.11:g.133364651_133364652del , CM000671.1:g.133364651_133364652del	GRCh37
NC_000009.10:g.132354472_132354473del	NCBI36
NG_011542.1:g.49558_49559del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.839-69_839-68del MANE Select	ENSP00000253004.6:n.839-69_839-68del
ENST00000352480.9:c.839-69_839-68del	ENSP00000253004.6:n.839-69_839-68del
ENST00000372386.6:n.110-69_110-68del
ENST00000372393.7:c.839-69_839-68del	ENSP00000361469.2:n.839-69_839-68del
ENST00000372394.5:c.839-69_839-68del	ENSP00000361471.1:n.839-69_839-68del
ENST00000470849.4:n.564-69_564-68del
ENST00000492400.5:n.348-69_348-68del
ENST00000493984.6:n.616-69_616-68del
NM_000050.4:c.839-69_839-68del	NP_000041.2:n.839-69_839-68del
NM_054012.3:c.839-69_839-68del	NP_446464.1:n.839-69_839-68del
XM_005272200.2:c.839-69_839-68del	XP_005272257.1:n.839-69_839-68del
XM_011518705.1:c.953-69_953-68del	XP_011517007.1:n.953-69_953-68del
XM_005272200.3:c.839-69_839-68del	XP_005272257.1:n.839-69_839-68del
XM_011518705.2:c.953-69_953-68del	XP_011517007.1:n.953-69_953-68del
XM_017014729.1:c.935-69_935-68del	XP_016870218.1:n.935-69_935-68del
NM_054012.4:c.839-69_839-68del MANE Select	NP_446464.1:n.839-69_839-68del