Canonical Allele Identifier: CA1768020115

Gene: ASAH1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18061490G= , CM000670.2:g.18061490G=	GRCh38
NC_000008.10:g.17918999G= , CM000670.1:g.17918999G=	GRCh37
NC_000008.9:g.17963279G=	NCBI36
NG_008985.1:g.28509C=
NG_008985.2:g.28509C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381733.9:c.752-32C=	ENSP00000371152.4:n.752-32C=
ENST00000517409.2:n.672-32C=
ENST00000518746.2:n.2358C=
ENST00000519545.6:n.721-32C=
ENST00000520781.6:c.629-32C=	ENSP00000427751.1:n.629-32C=
ENST00000521542.2:n.12-32C=
ENST00000635756.1:c.126-41C=
ENST00000635944.1:c.*540-32C=	ENSP00000490195.1:n.*540-32C=
ENST00000635998.1:c.704-32C=	ENSP00000490506.1:n.704-32C=
ENST00000636009.1:c.561-32C=	ENSP00000489988.1:n.561-32C=
ENST00000636033.1:c.*540-32C=	ENSP00000489617.1:n.*540-32C=
ENST00000636050.1:c.*547-32C=	ENSP00000490562.1:n.*547-32C=
ENST00000636128.1:c.383-32C=	ENSP00000489789.1:n.383-32C=
ENST00000636160.1:c.*596-32C=	ENSP00000489651.1:n.*596-32C=
ENST00000636171.1:c.647-32C=	ENSP00000489761.1:n.647-32C=
ENST00000636455.1:c.752-32C=	ENSP00000490502.1:n.752-32C=
ENST00000636494.1:c.*484-32C=	ENSP00000490388.1:n.*484-32C=
ENST00000636563.1:n.366-32C=
ENST00000636577.1:c.644-32C=	ENSP00000490027.1:n.644-32C=
ENST00000636691.1:c.509-32C=	ENSP00000490725.1:n.509-32C=
ENST00000636701.1:c.*355-32C=	ENSP00000489800.1:n.*355-32C=
ENST00000636815.1:c.621-32C=
ENST00000636920.1:c.*540-32C=	ENSP00000490437.1:n.*540-32C=
ENST00000636997.1:c.617-32C=	ENSP00000490093.1:n.617-32C=
ENST00000637013.1:c.*1072-32C=	ENSP00000490596.1:n.*1072-32C=
ENST00000637014.1:n.1111-32C=
ENST00000637095.1:c.*484-32C=	ENSP00000490415.1:n.*484-32C=
ENST00000637244.1:c.*1222-32C=	ENSP00000490188.1:n.*1222-32C=
ENST00000637343.1:n.2141-32C=
ENST00000637429.1:c.*916-32C=	ENSP00000490522.1:n.*916-32C=
ENST00000637484.1:c.*666-32C=	ENSP00000490837.1:n.*666-32C=
ENST00000637528.1:c.641-32C=	ENSP00000490801.1:n.641-32C=
ENST00000637609.1:n.3425-32C=
ENST00000637636.1:c.698-32C=	ENSP00000490112.1:n.698-32C=
ENST00000637790.2:c.704-32C= MANE Select	ENSP00000490272.1:n.704-32C=
ENST00000637857.1:n.1038C=
ENST00000637922.1:c.509-32C=	ENSP00000490071.1:n.509-32C=
ENST00000637991.1:c.677-32C=	ENSP00000489901.1:n.677-32C=
ENST00000638028.1:n.921-32C=
ENST00000638069.1:n.1493C=
ENST00000262097.10:c.704-32C=	ENSP00000262097.6:n.704-32C=
ENST00000314146.10:c.686-32C=	ENSP00000326970.10:n.686-32C=
ENST00000381733.8:c.752-32C=	ENSP00000371152.4:n.752-32C=
ENST00000518746.1:n.521-32C=
ENST00000519468.5:n.533-32C=
ENST00000520781.5:c.629-32C=	ENSP00000427751.1:n.629-32C=
ENST00000521542.1:n.385C=
NM_001127505.1:c.686-32C=	NP_001120977.1:n.686-32C=
NM_001127505.2:c.686-32C=	NP_001120977.1:n.686-32C=
NM_004315.4:c.752-32C=	NP_004306.3:n.752-32C=
NM_004315.5:c.752-32C=	NP_004306.3:n.752-32C=
NM_177924.3:c.704-32C=	NP_808592.2:n.704-32C=
NM_177924.4:c.704-32C=	NP_808592.2:n.704-32C=
XM_005273504.2:c.638-32C=	XP_005273561.1:n.638-32C=
NM_001363743.1:c.509-32C=	NP_001350672.1:n.509-32C=
XM_005273504.3:c.638-32C=	XP_005273561.1:n.638-32C=
NM_177924.5:c.704-32C= MANE Select	NP_808592.2:n.704-32C=
NM_001127505.3:c.686-32C=	NP_001120977.1:n.686-32C=
NM_001363743.2:c.509-32C=	NP_001350672.1:n.509-32C=
NM_004315.6:c.752-32C=	NP_004306.3:n.752-32C=