Canonical Allele Identifier: CA2683084132

Gene: ASL

Linked Data

• gnomAD v4: 7-66082230-C-CTGGGAGGGGGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66082231_66082232insGGGAGGGGGCAT , CM000669.2:g.66082231_66082232insGGGAGGGGGCAT	GRCh38
NC_000007.13:g.65547218_65547219insGGGAGGGGGCAT , CM000669.1:g.65547218_65547219insGGGAGGGGGCAT	GRCh37
NC_000007.12:g.65184653_65184654insGGGAGGGGGCAT	NCBI36
NG_009288.1:g.11443_11444insGGGAGGGGGCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.208-137_208-136insGGGAGGGGGCAT MANE Select	ENSP00000307188.9:n.208-137_208-136insGGGAGGGGGCAT
ENST00000362000.10:c.13-137_13-136insGGGAGGGGGCAT	ENSP00000354710.6:n.13-137_13-136insGGGAGGGGGCAT
ENST00000380839.9:c.208-137_208-136insGGGAGGGGGCAT	ENSP00000370219.4:n.208-137_208-136insGGGAGGGGGCAT
ENST00000395331.4:c.208-137_208-136insGGGAGGGGGCAT	ENSP00000378740.3:n.208-137_208-136insGGGAGGGGGCAT
ENST00000395332.8:c.208-137_208-136insGGGAGGGGGCAT	ENSP00000378741.3:n.208-137_208-136insGGGAGGGGGCAT
ENST00000671817.1:c.208-137_208-136insGGGAGGGGGCAT	ENSP00000500462.1:n.208-137_208-136insGGGAGGGGGCAT
ENST00000672498.1:c.208-137_208-136insGGGAGGGGGCAT	ENSP00000500227.1:n.208-137_208-136insGGGAGGGGGCAT
ENST00000672586.1:n.113-137_113-136insGGGAGGGGGCAT
ENST00000672676.1:n.378-137_378-136insGGGAGGGGGCAT
ENST00000673350.1:n.456-137_456-136insGGGAGGGGGCAT
ENST00000673518.1:c.208-137_208-136insGGGAGGGGGCAT	ENSP00000499889.1:n.208-137_208-136insGGGAGGGGGCAT
ENST00000673594.1:n.57-137_57-136insGGGAGGGGGCAT
ENST00000304874.13:c.208-137_208-136insGGGAGGGGGCAT	ENSP00000307188.9:n.208-137_208-136insGGGAGGGGGCAT
ENST00000362000.9:c.13-137_13-136insGGGAGGGGGCAT	ENSP00000354710.5:n.13-137_13-136insGGGAGGGGGCAT
ENST00000380839.8:c.208-137_208-136insGGGAGGGGGCAT	ENSP00000370219.4:n.208-137_208-136insGGGAGGGGGCAT
ENST00000395331.3:c.208-137_208-136insGGGAGGGGGCAT	ENSP00000378740.3:n.208-137_208-136insGGGAGGGGGCAT
ENST00000395332.7:c.208-137_208-136insGGGAGGGGGCAT	ENSP00000378741.3:n.208-137_208-136insGGGAGGGGGCAT
ENST00000487982.5:n.274-137_274-136insGGGAGGGGGCAT
ENST00000496336.1:n.449-137_449-136insGGGAGGGGGCAT
NM_000048.3:c.208-137_208-136insGGGAGGGGGCAT	NP_000039.2:n.208-137_208-136insGGGAGGGGGCAT
NM_001024943.1:c.208-137_208-136insGGGAGGGGGCAT	NP_001020114.1:n.208-137_208-136insGGGAGGGGGCAT
NM_001024944.1:c.208-137_208-136insGGGAGGGGGCAT	NP_001020115.1:n.208-137_208-136insGGGAGGGGGCAT
NM_001024946.1:c.208-137_208-136insGGGAGGGGGCAT	NP_001020117.1:n.208-137_208-136insGGGAGGGGGCAT
NM_000048.4:c.208-137_208-136insGGGAGGGGGCAT MANE Select	NP_000039.2:n.208-137_208-136insGGGAGGGGGCAT
NM_001024943.2:c.208-137_208-136insGGGAGGGGGCAT	NP_001020114.1:n.208-137_208-136insGGGAGGGGGCAT
NM_001024944.2:c.208-137_208-136insGGGAGGGGGCAT	NP_001020115.1:n.208-137_208-136insGGGAGGGGGCAT
NM_001024946.2:c.208-137_208-136insGGGAGGGGGCAT	NP_001020117.1:n.208-137_208-136insGGGAGGGGGCAT