Canonical Allele Identifier: CA2683086361

Gene: ASL

Linked Data

• gnomAD v4: 7-66087604-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66087608del , CM000669.2:g.66087608del	GRCh38
NC_000007.13:g.65552595del , CM000669.1:g.65552595del	GRCh37
NC_000007.12:g.65190030del	NCBI36
NG_009288.1:g.16820del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304874.14:c.656-121del MANE Select	ENSP00000307188.9:n.656-121del
ENST00000362000.10:c.461-121del	ENSP00000354710.6:n.461-121del
ENST00000380839.9:c.578-121del	ENSP00000370219.4:n.578-121del
ENST00000395331.4:c.656-121del	ENSP00000378740.3:n.656-121del
ENST00000395332.8:c.656-121del	ENSP00000378741.3:n.656-121del
ENST00000671817.1:c.578-121del	ENSP00000500462.1:n.578-121del
ENST00000672498.1:c.447-121del	ENSP00000500227.1:n.447-121del
ENST00000672586.1:n.1294del
ENST00000672676.1:n.1559del
ENST00000673149.1:n.468-121del
ENST00000673350.1:n.1637del
ENST00000673518.1:c.578-121del	ENSP00000499889.1:n.578-121del
ENST00000673594.1:n.726del
ENST00000304874.13:c.656-121del	ENSP00000307188.9:n.656-121del
ENST00000362000.9:c.461-121del	ENSP00000354710.5:n.461-121del
ENST00000380839.8:c.578-121del	ENSP00000370219.4:n.578-121del
ENST00000395331.3:c.656-121del	ENSP00000378740.3:n.656-121del
ENST00000395332.7:c.656-121del	ENSP00000378741.3:n.656-121del
NM_000048.3:c.656-121del	NP_000039.2:n.656-121del
NM_001024943.1:c.656-121del	NP_001020114.1:n.656-121del
NM_001024944.1:c.656-121del	NP_001020115.1:n.656-121del
NM_001024946.1:c.578-121del	NP_001020117.1:n.578-121del
NM_000048.4:c.656-121del MANE Select	NP_000039.2:n.656-121del
NM_001024943.2:c.656-121del	NP_001020114.1:n.656-121del
NM_001024944.2:c.656-121del	NP_001020115.1:n.656-121del
NM_001024946.2:c.578-121del	NP_001020117.1:n.578-121del