Canonical Allele Identifier: CA2695207750

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66087251_66087337del , CM000669.2:g.66087251_66087337del	GRCh38
NC_000007.13:g.65552238_65552324del , CM000669.1:g.65552238_65552324del	GRCh37
NC_000007.12:g.65189673_65189759del	NCBI36
NG_009288.1:g.16463_16549del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304874.14:c.603-83_606del
ENST00000362000.10:c.408-83_411del
ENST00000380839.9:c.525-83_528del
ENST00000395331.4:c.603-83_606del
ENST00000395332.8:c.603-83_606del
ENST00000671817.1:c.525-83_528del
ENST00000672498.1:c.447-478_447-392del	ENSP00000500227.1:n.447-478_447-392del
ENST00000672586.1:n.937_1023del
ENST00000672676.1:n.1202_1288del
ENST00000673149.1:n.415-83_418del
ENST00000673350.1:n.1280_1366del
ENST00000673518.1:c.525-83_528del
ENST00000673594.1:n.452-83_455del
ENST00000304874.13:c.603-83_606del
ENST00000362000.9:c.408-83_411del
ENST00000380839.8:c.525-83_528del
ENST00000395331.3:c.603-83_606del
ENST00000395332.7:c.603-83_606del
NM_000048.3:c.603-83_606del
NM_001024943.1:c.603-83_606del
NM_001024944.1:c.603-83_606del
NM_001024946.1:c.525-83_528del
NM_000048.4:c.603-83_606del
NM_001024943.2:c.603-83_606del
NM_001024944.2:c.603-83_606del
NM_001024946.2:c.525-83_528del