Canonical Allele Identifier: CA574859583
Gene: ASL HGNC NCBI

Linked Data

dbSNP Id: rs1489077698
gnomAD v2: 7-65557115-G-C
gnomAD v4: 7-66092128-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66092128G>C , CM000669.2:g.66092128G>C GRCh38
NC_000007.13:g.65557115G>C , CM000669.1:g.65557115G>C GRCh37
NC_000007.12:g.65194550G>C NCBI36
NG_009288.1:g.21340G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000304874.14:c.1143+42G>C MANE Select ENSP00000307188.9:n.1143+42G>C
ENST00000362000.10:c.948+42G>C ENSP00000354710.6:n.948+42G>C
ENST00000380839.9:c.1065+42G>C ENSP00000370219.4:n.1065+42G>C
ENST00000395331.4:c.1083+42G>C ENSP00000378740.3:n.1083+42G>C
ENST00000395332.8:c.1143+42G>C ENSP00000378741.3:n.1143+42G>C
ENST00000488343.2:c.148-776G>C ENSP00000500864.1:n.148-776G>C
ENST00000672498.1:c.*442+42G>C ENSP00000500227.1:n.*442+42G>C
ENST00000672586.1:n.1902+42G>C
ENST00000672676.1:n.2167+42G>C
ENST00000673149.1:n.955+42G>C
ENST00000673350.1:n.3260+42G>C
ENST00000673518.1:c.1065+42G>C ENSP00000499889.1:n.1065+42G>C
ENST00000304874.13:c.1143+42G>C ENSP00000307188.9:n.1143+42G>C
ENST00000380839.8:c.1065+42G>C ENSP00000370219.4:n.1065+42G>C
ENST00000395331.3:c.1083+42G>C ENSP00000378740.3:n.1083+42G>C
ENST00000395332.7:c.1143+42G>C ENSP00000378741.3:n.1143+42G>C
ENST00000450043.2:c.456+42G>C ENSP00000396527.2:n.456+42G>C
ENST00000464970.1:n.346+42G>C
ENST00000488343.1:n.148-776G>C
ENST00000493708.5:n.624+42G>C
NM_000048.3:c.1143+42G>C NP_000039.2:n.1143+42G>C
NM_001024943.1:c.1143+42G>C NP_001020114.1:n.1143+42G>C
NM_001024944.1:c.1083+42G>C NP_001020115.1:n.1083+42G>C
NM_001024946.1:c.1065+42G>C NP_001020117.1:n.1065+42G>C
NM_000048.4:c.1143+42G>C MANE Select NP_000039.2:n.1143+42G>C
NM_001024943.2:c.1143+42G>C NP_001020114.1:n.1143+42G>C
NM_001024944.2:c.1083+42G>C NP_001020115.1:n.1083+42G>C
NM_001024946.2:c.1065+42G>C NP_001020117.1:n.1065+42G>C