Canonical Allele Identifier: CA574858936

Gene: ASL

Linked Data

• dbSNP Id: rs1370830986
• gnomAD v2: 7-65551830-C-G
• gnomAD v4: 7-66086843-C-G
• MyVariant Identifiers: chr7:g.65551830C>G (hg19) ; chr7:g.66086843C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66086843C>G , CM000669.2:g.66086843C>G	GRCh38
NC_000007.13:g.65551830C>G , CM000669.1:g.65551830C>G	GRCh37
NC_000007.12:g.65189265C>G	NCBI36
NG_009288.1:g.16055C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000304874.14:c.602+22C>G MANE Select	ENSP00000307188.9:n.602+22C>G
ENST00000362000.10:c.407+22C>G	ENSP00000354710.6:n.407+22C>G
ENST00000380839.9:c.524+181C>G	ENSP00000370219.4:n.524+181C>G
ENST00000395331.4:c.602+22C>G	ENSP00000378740.3:n.602+22C>G
ENST00000395332.8:c.602+22C>G	ENSP00000378741.3:n.602+22C>G
ENST00000671817.1:c.524+181C>G	ENSP00000500462.1:n.524+181C>G
ENST00000672498.1:c.447-886C>G	ENSP00000500227.1:n.447-886C>G
ENST00000672586.1:n.529C>G
ENST00000672676.1:n.794C>G
ENST00000673149.1:n.414+22C>G
ENST00000673350.1:n.872C>G
ENST00000673518.1:c.524+181C>G	ENSP00000499889.1:n.524+181C>G
ENST00000673594.1:n.451+22C>G
ENST00000304874.13:c.602+22C>G	ENSP00000307188.9:n.602+22C>G
ENST00000362000.9:c.407+22C>G	ENSP00000354710.5:n.407+22C>G
ENST00000380839.8:c.524+181C>G	ENSP00000370219.4:n.524+181C>G
ENST00000395331.3:c.602+22C>G	ENSP00000378740.3:n.602+22C>G
ENST00000395332.7:c.602+22C>G	ENSP00000378741.3:n.602+22C>G
ENST00000487982.5:n.690C>G
NM_000048.3:c.602+22C>G	NP_000039.2:n.602+22C>G
NM_001024943.1:c.602+22C>G	NP_001020114.1:n.602+22C>G
NM_001024944.1:c.602+22C>G	NP_001020115.1:n.602+22C>G
NM_001024946.1:c.524+181C>G	NP_001020117.1:n.524+181C>G
NM_000048.4:c.602+22C>G MANE Select	NP_000039.2:n.602+22C>G
NM_001024943.2:c.602+22C>G	NP_001020114.1:n.602+22C>G
NM_001024944.2:c.602+22C>G	NP_001020115.1:n.602+22C>G
NM_001024946.2:c.524+181C>G	NP_001020117.1:n.524+181C>G