Canonical Allele Identifier: CA2692120552

Gene: ASS1

Linked Data

• gnomAD v4: 9-130458385-GCTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130458389_130458391del , CM000671.2:g.130458389_130458391del	GRCh38
NC_000009.11:g.133333776_133333778del , CM000671.1:g.133333776_133333778del	GRCh37
NC_000009.10:g.132323597_132323599del	NCBI36
NG_011542.1:g.18683_18685del

Transcript Alleles

HGVS	Amino-acid change
ENST00000352480.10:c.175-12_175-10del MANE Select	ENSP00000253004.6:n.175-12_175-10del
ENST00000352480.9:c.175-12_175-10del	ENSP00000253004.6:n.175-12_175-10del
ENST00000372393.7:c.175-12_175-10del	ENSP00000361469.2:n.175-12_175-10del
ENST00000372394.5:c.175-12_175-10del	ENSP00000361471.1:n.175-12_175-10del
ENST00000422569.5:c.175-12_175-10del	ENSP00000394212.1:n.175-12_175-10del
ENST00000443588.1:c.175-12_175-10del	ENSP00000397785.1:n.175-12_175-10del
NM_000050.4:c.175-12_175-10del	NP_000041.2:n.175-12_175-10del
NM_054012.3:c.175-12_175-10del	NP_446464.1:n.175-12_175-10del
XM_005272200.2:c.175-12_175-10del	XP_005272257.1:n.175-12_175-10del
XM_011518705.1:c.289-12_289-10del	XP_011517007.1:n.289-12_289-10del
XM_005272200.3:c.175-12_175-10del	XP_005272257.1:n.175-12_175-10del
XM_011518705.2:c.289-12_289-10del	XP_011517007.1:n.289-12_289-10del
XM_017014729.1:c.271-12_271-10del	XP_016870218.1:n.271-12_271-10del
NM_054012.4:c.175-12_175-10del MANE Select	NP_446464.1:n.175-12_175-10del