Canonical Allele Identifier: CA1713927832
Gene: ASL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66092188_66092189delinsAC , CM000669.2:g.66092188_66092189delinsAC GRCh38
NC_000007.13:g.65557175_65557176delinsAC , CM000669.1:g.65557175_65557176delinsAC GRCh37
NC_000007.12:g.65194610_65194611delinsAC NCBI36
NG_009288.1:g.21400_21401delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000304874.14:c.1143+102_1143+103delinsAC MANE Select ENSP00000307188.9:n.1143+102_1143+103delinsAC
ENST00000362000.10:c.948+102_948+103delinsAC ENSP00000354710.6:n.948+102_948+103delinsAC
ENST00000380839.9:c.1065+102_1065+103delinsAC ENSP00000370219.4:n.1065+102_1065+103delinsAC
ENST00000395331.4:c.1083+102_1083+103delinsAC ENSP00000378740.3:n.1083+102_1083+103delinsAC
ENST00000395332.8:c.1143+102_1143+103delinsAC ENSP00000378741.3:n.1143+102_1143+103delinsAC
ENST00000488343.2:c.148-716_148-715delinsAC ENSP00000500864.1:n.148-716_148-715delinsAC
ENST00000672498.1:c.*442+102_*442+103delinsAC ENSP00000500227.1:n.*442+102_*442+103delinsAC
ENST00000672586.1:n.1902+102_1902+103delinsAC
ENST00000672676.1:n.2167+102_2167+103delinsAC
ENST00000673149.1:n.955+102_955+103delinsAC
ENST00000673350.1:n.3260+102_3260+103delinsAC
ENST00000673518.1:c.1065+102_1065+103delinsAC ENSP00000499889.1:n.1065+102_1065+103delinsAC
ENST00000304874.13:c.1143+102_1143+103delinsAC ENSP00000307188.9:n.1143+102_1143+103delinsAC
ENST00000380839.8:c.1065+102_1065+103delinsAC ENSP00000370219.4:n.1065+102_1065+103delinsAC
ENST00000395331.3:c.1083+102_1083+103delinsAC ENSP00000378740.3:n.1083+102_1083+103delinsAC
ENST00000395332.7:c.1143+102_1143+103delinsAC ENSP00000378741.3:n.1143+102_1143+103delinsAC
ENST00000450043.2:c.456+102_456+103delinsAC ENSP00000396527.2:n.456+102_456+103delinsAC
ENST00000464970.1:n.346+102_346+103delinsAC
ENST00000488343.1:n.148-716_148-715delinsAC
ENST00000493708.5:n.624+102_624+103delinsAC
NM_000048.3:c.1143+102_1143+103delinsAC NP_000039.2:n.1143+102_1143+103delinsAC
NM_001024943.1:c.1143+102_1143+103delinsAC NP_001020114.1:n.1143+102_1143+103delinsAC
NM_001024944.1:c.1083+102_1083+103delinsAC NP_001020115.1:n.1083+102_1083+103delinsAC
NM_001024946.1:c.1065+102_1065+103delinsAC NP_001020117.1:n.1065+102_1065+103delinsAC
NM_000048.4:c.1143+102_1143+103delinsAC MANE Select NP_000039.2:n.1143+102_1143+103delinsAC
NM_001024943.2:c.1143+102_1143+103delinsAC NP_001020114.1:n.1143+102_1143+103delinsAC
NM_001024944.2:c.1083+102_1083+103delinsAC NP_001020115.1:n.1083+102_1083+103delinsAC
NM_001024946.2:c.1065+102_1065+103delinsAC NP_001020117.1:n.1065+102_1065+103delinsAC