Canonical Allele Identifier: CA1713923459

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66089199_66089207delinsGGGGCCTCT , CM000669.2:g.66089199_66089207delinsGGGGCCTCT	GRCh38
NC_000007.13:g.65554186_65554194delinsGGGGCCTCT , CM000669.1:g.65554186_65554194delinsGGGGCCTCT	GRCh37
NC_000007.12:g.65191621_65191629delinsGGGGCCTCT	NCBI36
NG_009288.1:g.18411_18419delinsGGGGCCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.918+24_918+32delinsGGGGCCTCT MANE Select	ENSP00000307188.9:n.918+24_918+32delinsGGGGCCTCT
ENST00000362000.10:c.723+24_723+32delinsGGGGCCTCT	ENSP00000354710.6:n.723+24_723+32delinsGGGGCCTCT
ENST00000380839.9:c.840+24_840+32delinsGGGGCCTCT	ENSP00000370219.4:n.840+24_840+32delinsGGGGCCTCT
ENST00000395331.4:c.918+24_918+32delinsGGGGCCTCT	ENSP00000378740.3:n.918+24_918+32delinsGGGGCCTCT
ENST00000395332.8:c.918+24_918+32delinsGGGGCCTCT	ENSP00000378741.3:n.918+24_918+32delinsGGGGCCTCT
ENST00000488343.2:c.87+24_87+32delinsGGGGCCTCT	ENSP00000500864.1:n.87+24_87+32delinsGGGGCCTCT
ENST00000671817.1:c.840+24_840+32delinsGGGGCCTCT	ENSP00000500462.1:n.840+24_840+32delinsGGGGCCTCT
ENST00000672498.1:c.*217+24_*217+32delinsGGGGCCTCT	ENSP00000500227.1:n.*217+24_*217+32delinsGGGGCCTCT
ENST00000672586.1:n.1677+24_1677+32delinsGGGGCCTCT
ENST00000672676.1:n.1942+24_1942+32delinsGGGGCCTCT
ENST00000673149.1:n.730+24_730+32delinsGGGGCCTCT
ENST00000673350.1:n.3035+24_3035+32delinsGGGGCCTCT
ENST00000673518.1:c.840+24_840+32delinsGGGGCCTCT	ENSP00000499889.1:n.840+24_840+32delinsGGGGCCTCT
ENST00000304874.13:c.918+24_918+32delinsGGGGCCTCT	ENSP00000307188.9:n.918+24_918+32delinsGGGGCCTCT
ENST00000380839.8:c.840+24_840+32delinsGGGGCCTCT	ENSP00000370219.4:n.840+24_840+32delinsGGGGCCTCT
ENST00000395331.3:c.918+24_918+32delinsGGGGCCTCT	ENSP00000378740.3:n.918+24_918+32delinsGGGGCCTCT
ENST00000395332.7:c.918+24_918+32delinsGGGGCCTCT	ENSP00000378741.3:n.918+24_918+32delinsGGGGCCTCT
ENST00000450043.2:c.231+24_231+32delinsGGGGCCTCT	ENSP00000396527.2:n.231+24_231+32delinsGGGGCCTCT
ENST00000488343.1:n.87+24_87+32delinsGGGGCCTCT
ENST00000493708.5:n.323_331delinsGGGGCCTCT
NM_000048.3:c.918+24_918+32delinsGGGGCCTCT	NP_000039.2:n.918+24_918+32delinsGGGGCCTCT
NM_001024943.1:c.918+24_918+32delinsGGGGCCTCT	NP_001020114.1:n.918+24_918+32delinsGGGGCCTCT
NM_001024944.1:c.918+24_918+32delinsGGGGCCTCT	NP_001020115.1:n.918+24_918+32delinsGGGGCCTCT
NM_001024946.1:c.840+24_840+32delinsGGGGCCTCT	NP_001020117.1:n.840+24_840+32delinsGGGGCCTCT
NM_000048.4:c.918+24_918+32delinsGGGGCCTCT MANE Select	NP_000039.2:n.918+24_918+32delinsGGGGCCTCT
NM_001024943.2:c.918+24_918+32delinsGGGGCCTCT	NP_001020114.1:n.918+24_918+32delinsGGGGCCTCT
NM_001024944.2:c.918+24_918+32delinsGGGGCCTCT	NP_001020115.1:n.918+24_918+32delinsGGGGCCTCT
NM_001024946.2:c.840+24_840+32delinsGGGGCCTCT	NP_001020117.1:n.840+24_840+32delinsGGGGCCTCT