Canonical Allele Identifier: CA4277402

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66092883C>T , CM000669.2:g.66092883C>T	GRCh38
NC_000007.13:g.65557870C>T , CM000669.1:g.65557870C>T	GRCh37
NC_000007.12:g.65195305C>T	NCBI36
NG_009288.1:g.22095C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000048.4:c.1366C>T MANE Select	NP_000039.2:p.Arg456Trp
ENST00000304874.14:c.1366C>T MANE Select	ENSP00000307188.9:p.Arg456Trp
NM_000048.3:c.1366C>T	NP_000039.2:p.Arg456Trp
NM_001024943.1:c.1366C>T	NP_001020114.1:p.Arg456Trp
NM_001024943.2:c.1366C>T	NP_001020114.1:p.Arg456Trp
NM_001024944.1:c.1306C>T	NP_001020115.1:p.Arg436Trp
NM_001024944.2:c.1306C>T	NP_001020115.1:p.Arg436Trp
NM_001024946.1:c.1288C>T	NP_001020117.1:p.Arg430Trp
NM_001024946.2:c.1288C>T	NP_001020117.1:p.Arg430Trp
ENST00000304874.13:c.1366C>T	ENSP00000307188.9:p.Arg456Trp
ENST00000362000.10:c.1171C>T	ENSP00000354710.6:p.Arg391Trp
ENST00000380839.8:c.1288C>T	ENSP00000370219.4:p.Arg430Trp
ENST00000380839.9:c.1288C>T	ENSP00000370219.4:p.Arg430Trp
ENST00000395331.3:c.1306C>T	ENSP00000378740.3:p.Arg436Trp
ENST00000395331.4:c.1306C>T	ENSP00000378740.3:p.Arg436Trp
ENST00000395332.7:c.1366C>T	ENSP00000378741.3:p.Arg456Trp
ENST00000395332.8:c.1366C>T	ENSP00000378741.3:p.Arg456Trp
ENST00000450043.2:c.563+220C>T	ENSP00000396527.2:n.563+220C>T
ENST00000464970.1:n.569C>T
ENST00000488343.1:n.148-21C>T
ENST00000488343.2:c.148-21C>T	ENSP00000500864.1:n.148-21C>T
ENST00000493708.5:n.847C>T
ENST00000672498.1:c.*769C>T	ENSP00000500227.1:n.*769C>T
ENST00000672586.1:n.2125C>T
ENST00000672676.1:n.2390C>T
ENST00000673149.1:n.1178C>T
ENST00000673350.1:n.3483C>T
ENST00000673518.1:c.1288C>T	ENSP00000499889.1:p.Arg430Trp