Canonical Allele Identifier: CA370431776

Gene: ASAH1

Linked Data

• gnomAD v4: 8-18064514-T-A
• MyVariant Identifiers: chr8:g.17922023T>A (hg19) ; chr8:g.18064514T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18064514T>A , CM000670.2:g.18064514T>A	GRCh38
NC_000008.10:g.17922023T>A , CM000670.1:g.17922023T>A	GRCh37
NC_000008.9:g.17966303T>A	NCBI36
NG_008985.1:g.25485A>T
NG_008985.2:g.25485A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381733.9:c.448A>T	ENSP00000371152.4:p.Asn150Tyr
ENST00000519545.6:n.417A>T
ENST00000520781.6:c.383-1284A>T	ENSP00000427751.1:n.383-1284A>T
ENST00000523593.6:c.*243A>T	ENSP00000490700.1:n.*243A>T
ENST00000523744.2:n.4158A>T
ENST00000635769.1:c.421A>T	ENSP00000490485.1:p.Asn141Tyr
ENST00000635944.1:c.*236A>T	ENSP00000490195.1:n.*236A>T
ENST00000635998.1:c.400A>T	ENSP00000490506.1:p.Asn134Tyr
ENST00000636009.1:c.315-1284A>T	ENSP00000489988.1:n.315-1284A>T
ENST00000636033.1:c.*236A>T	ENSP00000489617.1:n.*236A>T
ENST00000636050.1:c.*243A>T	ENSP00000490562.1:n.*243A>T
ENST00000636128.1:c.382+2706A>T	ENSP00000489789.1:n.382+2706A>T
ENST00000636160.1:c.*292A>T	ENSP00000489651.1:n.*292A>T
ENST00000636171.1:c.383-40A>T	ENSP00000489761.1:n.383-40A>T
ENST00000636299.1:c.*171A>T	ENSP00000490202.1:n.*171A>T
ENST00000636435.1:n.3172A>T
ENST00000636455.1:c.448A>T	ENSP00000490502.1:p.Asn150Tyr
ENST00000636494.1:c.*180A>T	ENSP00000490388.1:n.*180A>T
ENST00000636563.1:n.62A>T
ENST00000636577.1:c.383-43A>T	ENSP00000490027.1:n.383-43A>T
ENST00000636691.1:c.205A>T	ENSP00000490725.1:p.Asn69Tyr
ENST00000636701.1:c.*51A>T	ENSP00000489800.1:n.*51A>T
ENST00000636815.1:c.317A>T
ENST00000636823.1:c.205A>T	ENSP00000490798.1:p.Asn69Tyr
ENST00000636828.1:n.3264A>T
ENST00000636920.1:c.*236A>T	ENSP00000490437.1:n.*236A>T
ENST00000636997.1:c.313A>T	ENSP00000490093.1:p.Asn105Tyr
ENST00000637013.1:c.*612A>T	ENSP00000490596.1:n.*612A>T
ENST00000637095.1:c.*180A>T	ENSP00000490415.1:n.*180A>T
ENST00000637244.1:c.*918A>T	ENSP00000490188.1:n.*918A>T
ENST00000637343.1:n.611A>T
ENST00000637429.1:c.*612A>T	ENSP00000490522.1:n.*612A>T
ENST00000637484.1:c.*420-1284A>T	ENSP00000490837.1:n.*420-1284A>T
ENST00000637528.1:c.383-46A>T	ENSP00000490801.1:n.383-46A>T
ENST00000637603.1:c.370A>T	ENSP00000489979.1:p.Asn124Tyr
ENST00000637609.1:n.3121A>T
ENST00000637636.1:c.394A>T	ENSP00000490112.1:p.Asn132Tyr
ENST00000637638.1:c.400A>T	ENSP00000490774.1:p.Asn134Tyr
ENST00000637718.1:c.205A>T	ENSP00000490133.1:p.Asn69Tyr
ENST00000637790.2:c.400A>T MANE Select	ENSP00000490272.1:p.Asn134Tyr
ENST00000637857.1:n.105-2091A>T
ENST00000637922.1:c.205A>T	ENSP00000490071.1:p.Asn69Tyr
ENST00000637991.1:c.431-1284A>T	ENSP00000489901.1:n.431-1284A>T
ENST00000638069.1:n.456A>T
ENST00000262097.10:c.400A>T	ENSP00000262097.6:p.Asn134Tyr
ENST00000314146.10:c.382A>T	ENSP00000326970.10:p.Asn128Tyr
ENST00000381733.8:c.448A>T	ENSP00000371152.4:p.Asn150Tyr
ENST00000519468.5:n.389-2147A>T
ENST00000519545.5:n.414A>T
ENST00000520781.5:c.383-1284A>T	ENSP00000427751.1:n.383-1284A>T
ENST00000523593.5:n.253A>T
ENST00000523744.1:n.403A>T
NM_001127505.1:c.382A>T	NP_001120977.1:p.Asn128Tyr
NM_001127505.2:c.382A>T	NP_001120977.1:p.Asn128Tyr
NM_004315.4:c.448A>T	NP_004306.3:p.Asn150Tyr
NM_004315.5:c.448A>T	NP_004306.3:p.Asn150Tyr
NM_177924.3:c.400A>T	NP_808592.2:p.Asn134Tyr
NM_177924.4:c.400A>T	NP_808592.2:p.Asn134Tyr
XM_005273504.2:c.334A>T	XP_005273561.1:p.Asn112Tyr
NM_001363743.1:c.205A>T	NP_001350672.1:p.Asn69Tyr
XM_005273504.3:c.334A>T	XP_005273561.1:p.Asn112Tyr
NM_177924.5:c.400A>T MANE Select	NP_808592.2:p.Asn134Tyr
NM_001127505.3:c.382A>T	NP_001120977.1:p.Asn128Tyr
NM_001363743.2:c.205A>T	NP_001350672.1:p.Asn69Tyr
NM_004315.6:c.448A>T	NP_004306.3:p.Asn150Tyr