Canonical Allele Identifier: CA2599088714

Gene: ASL

Linked Data

• dbSNP Id: rs2115701064
• gnomAD v3: 7-66083195-CA-C
• gnomAD v4: 7-66083195-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66083196del , CM000669.2:g.66083196del	GRCh38
NC_000007.13:g.65548183del , CM000669.1:g.65548183del	GRCh37
NC_000007.12:g.65185618del	NCBI36
NG_009288.1:g.12408del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.446+22del MANE Select	ENSP00000307188.9:n.446+22del
ENST00000362000.10:c.251+22del	ENSP00000354710.6:n.251+22del
ENST00000380839.9:c.446+22del	ENSP00000370219.4:n.446+22del
ENST00000395331.4:c.446+22del	ENSP00000378740.3:n.446+22del
ENST00000395332.8:c.446+22del	ENSP00000378741.3:n.446+22del
ENST00000671817.1:c.446+22del	ENSP00000500462.1:n.446+22del
ENST00000672498.1:c.446+22del	ENSP00000500227.1:n.446+22del
ENST00000672586.1:n.351+22del
ENST00000672676.1:n.616+22del
ENST00000673149.1:n.258+22del
ENST00000673350.1:n.694+22del
ENST00000673518.1:c.446+22del	ENSP00000499889.1:n.446+22del
ENST00000673594.1:n.295+22del
ENST00000304874.13:c.446+22del	ENSP00000307188.9:n.446+22del
ENST00000362000.9:c.251+22del	ENSP00000354710.5:n.251+22del
ENST00000380839.8:c.446+22del	ENSP00000370219.4:n.446+22del
ENST00000395331.3:c.446+22del	ENSP00000378740.3:n.446+22del
ENST00000395332.7:c.446+22del	ENSP00000378741.3:n.446+22del
ENST00000487982.5:n.512+22del
ENST00000496336.1:n.849del
NM_000048.3:c.446+22del	NP_000039.2:n.446+22del
NM_001024943.1:c.446+22del	NP_001020114.1:n.446+22del
NM_001024944.1:c.446+22del	NP_001020115.1:n.446+22del
NM_001024946.1:c.446+22del	NP_001020117.1:n.446+22del
NM_000048.4:c.446+22del MANE Select	NP_000039.2:n.446+22del
NM_001024943.2:c.446+22del	NP_001020114.1:n.446+22del
NM_001024944.2:c.446+22del	NP_001020115.1:n.446+22del
NM_001024946.2:c.446+22del	NP_001020117.1:n.446+22del