Canonical Allele Identifier: CA1713927398
Gene: ASL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66092022T= , CM000669.2:g.66092022T= GRCh38
NC_000007.13:g.65557009T= , CM000669.1:g.65557009T= GRCh37
NC_000007.12:g.65194444T= NCBI36
NG_009288.1:g.21234T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304874.14:c.1079T= MANE Select ENSP00000307188.9:p.Met360=
ENST00000362000.10:c.884T= ENSP00000354710.6:p.Met295=
ENST00000380839.9:c.1001T= ENSP00000370219.4:p.Met334=
ENST00000395331.4:c.1019T= ENSP00000378740.3:p.Met340=
ENST00000395332.8:c.1079T= ENSP00000378741.3:p.Met360=
ENST00000488343.2:c.148-882T= ENSP00000500864.1:n.148-882T=
ENST00000671817.1:c.1001T= ENSP00000500462.1:p.Met334=
ENST00000672498.1:c.*378T= ENSP00000500227.1:n.*378T=
ENST00000672586.1:n.1838T=
ENST00000672676.1:n.2103T=
ENST00000673149.1:n.891T=
ENST00000673350.1:n.3196T=
ENST00000673518.1:c.1001T= ENSP00000499889.1:p.Met334=
ENST00000304874.13:c.1079T= ENSP00000307188.9:p.Met360=
ENST00000380839.8:c.1001T= ENSP00000370219.4:p.Met334=
ENST00000395331.3:c.1019T= ENSP00000378740.3:p.Met340=
ENST00000395332.7:c.1079T= ENSP00000378741.3:p.Met360=
ENST00000450043.2:c.392T= ENSP00000396527.2:p.Met131=
ENST00000464970.1:n.282T=
ENST00000488343.1:n.148-882T=
ENST00000493708.5:n.560T=
NM_000048.3:c.1079T= NP_000039.2:p.Met360=
NM_001024943.1:c.1079T= NP_001020114.1:p.Met360=
NM_001024944.1:c.1019T= NP_001020115.1:p.Met340=
NM_001024946.1:c.1001T= NP_001020117.1:p.Met334=
NM_000048.4:c.1079T= MANE Select NP_000039.2:p.Met360=
NM_001024943.2:c.1079T= NP_001020114.1:p.Met360=
NM_001024944.2:c.1019T= NP_001020115.1:p.Met340=
NM_001024946.2:c.1001T= NP_001020117.1:p.Met334=