Canonical Allele Identifier: CA4277007

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66086790C>T , CM000669.2:g.66086790C>T	GRCh38
NC_000007.13:g.65551777C>T , CM000669.1:g.65551777C>T	GRCh37
NC_000007.12:g.65189212C>T	NCBI36
NG_009288.1:g.16002C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000048.4:c.571C>T MANE Select	NP_000039.2:p.Arg191Trp
ENST00000304874.14:c.571C>T MANE Select	ENSP00000307188.9:p.Arg191Trp
NM_000048.3:c.571C>T	NP_000039.2:p.Arg191Trp
NM_001024943.1:c.571C>T	NP_001020114.1:p.Arg191Trp
NM_001024943.2:c.571C>T	NP_001020114.1:p.Arg191Trp
NM_001024944.1:c.571C>T	NP_001020115.1:p.Arg191Trp
NM_001024944.2:c.571C>T	NP_001020115.1:p.Arg191Trp
NM_001024946.1:c.524+128C>T	NP_001020117.1:n.524+128C>T
NM_001024946.2:c.524+128C>T	NP_001020117.1:n.524+128C>T
ENST00000304874.13:c.571C>T	ENSP00000307188.9:p.Arg191Trp
ENST00000362000.10:c.376C>T	ENSP00000354710.6:p.Arg126Trp
ENST00000362000.9:c.376C>T	ENSP00000354710.5:p.Arg126Trp
ENST00000380839.8:c.524+128C>T	ENSP00000370219.4:n.524+128C>T
ENST00000380839.9:c.524+128C>T	ENSP00000370219.4:n.524+128C>T
ENST00000395331.3:c.571C>T	ENSP00000378740.3:p.Arg191Trp
ENST00000395331.4:c.571C>T	ENSP00000378740.3:p.Arg191Trp
ENST00000395332.7:c.571C>T	ENSP00000378741.3:p.Arg191Trp
ENST00000395332.8:c.571C>T	ENSP00000378741.3:p.Arg191Trp
ENST00000487982.5:n.637C>T
ENST00000671817.1:c.524+128C>T	ENSP00000500462.1:n.524+128C>T
ENST00000672498.1:c.447-939C>T	ENSP00000500227.1:n.447-939C>T
ENST00000672586.1:n.476C>T
ENST00000672676.1:n.741C>T
ENST00000673149.1:n.383C>T
ENST00000673350.1:n.819C>T
ENST00000673518.1:c.524+128C>T	ENSP00000499889.1:n.524+128C>T
ENST00000673594.1:n.420C>T