Canonical Allele Identifier: CA4276817

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66081852T>C , CM000669.2:g.66081852T>C	GRCh38
NC_000007.13:g.65546839T>C , CM000669.1:g.65546839T>C	GRCh37
NC_000007.12:g.65184274T>C	NCBI36
NG_009288.1:g.11064T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000048.4:c.62T>C MANE Select	NP_000039.2:p.Met21Thr
ENST00000304874.14:c.62T>C MANE Select	ENSP00000307188.9:p.Met21Thr
NM_000048.3:c.62T>C	NP_000039.2:p.Met21Thr
NM_001024943.1:c.62T>C	NP_001020114.1:p.Met21Thr
NM_001024943.2:c.62T>C	NP_001020114.1:p.Met21Thr
NM_001024944.1:c.62T>C	NP_001020115.1:p.Met21Thr
NM_001024944.2:c.62T>C	NP_001020115.1:p.Met21Thr
NM_001024946.1:c.62T>C	NP_001020117.1:p.Met21Thr
NM_001024946.2:c.62T>C	NP_001020117.1:p.Met21Thr
ENST00000304874.13:c.62T>C	ENSP00000307188.9:p.Met21Thr
ENST00000362000.10:c.13-516T>C	ENSP00000354710.6:n.13-516T>C
ENST00000362000.9:c.13-516T>C	ENSP00000354710.5:n.13-516T>C
ENST00000380839.8:c.62T>C	ENSP00000370219.4:p.Met21Thr
ENST00000380839.9:c.62T>C	ENSP00000370219.4:p.Met21Thr
ENST00000395331.3:c.62T>C	ENSP00000378740.3:p.Met21Thr
ENST00000395331.4:c.62T>C	ENSP00000378740.3:p.Met21Thr
ENST00000395332.7:c.62T>C	ENSP00000378741.3:p.Met21Thr
ENST00000395332.8:c.62T>C	ENSP00000378741.3:p.Met21Thr
ENST00000487982.5:n.128T>C
ENST00000496336.1:n.303T>C
ENST00000671817.1:c.62T>C	ENSP00000500462.1:p.Met21Thr
ENST00000672498.1:c.62T>C	ENSP00000500227.1:p.Met21Thr
ENST00000672586.1:n.113-516T>C
ENST00000672676.1:n.232T>C
ENST00000673350.1:n.310T>C
ENST00000673518.1:c.62T>C	ENSP00000499889.1:p.Met21Thr