Canonical Allele Identifier: CA2540962433

Gene: ASAH1

Linked Data

• gnomAD v4: 8-18057191-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18057191C>A , CM000670.2:g.18057191C>A	GRCh38
NC_000008.10:g.17914700C>A , CM000670.1:g.17914700C>A	GRCh37
NC_000008.9:g.17958980C>A	NCBI36
NG_008985.1:g.32808G>T
NG_008985.2:g.32808G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000381733.9:c.*343G>T	ENSP00000371152.4:n.*343G>T
ENST00000518746.2:n.3217G>T
ENST00000520781.6:c.*343G>T	ENSP00000427751.1:n.*343G>T
ENST00000635756.1:c.944G>T
ENST00000635944.1:c.*1367G>T	ENSP00000490195.1:n.*1367G>T
ENST00000635998.1:c.*244G>T	ENSP00000490506.1:n.*244G>T
ENST00000636009.1:c.1388G>T	ENSP00000489988.1:n.1388G>T
ENST00000636033.1:c.*1367G>T	ENSP00000489617.1:n.*1367G>T
ENST00000636050.1:c.*1374G>T	ENSP00000490562.1:n.*1374G>T
ENST00000636128.1:c.*343G>T	ENSP00000489789.1:n.*343G>T
ENST00000636160.1:c.*1423G>T	ENSP00000489651.1:n.*1423G>T
ENST00000636171.1:c.*343G>T	ENSP00000489761.1:n.*343G>T
ENST00000636455.1:c.*429G>T	ENSP00000490502.1:n.*429G>T
ENST00000636494.1:c.*1311G>T	ENSP00000490388.1:n.*1311G>T
ENST00000636563.1:n.1193G>T
ENST00000636577.1:c.*343G>T	ENSP00000490027.1:n.*343G>T
ENST00000636691.1:c.*343G>T	ENSP00000490725.1:n.*343G>T
ENST00000636701.1:c.*1182G>T	ENSP00000489800.1:n.*1182G>T
ENST00000636815.1:c.1448G>T
ENST00000636920.1:c.*1367G>T	ENSP00000490437.1:n.*1367G>T
ENST00000636997.1:c.*343G>T	ENSP00000490093.1:n.*343G>T
ENST00000637013.1:c.*1899G>T	ENSP00000490596.1:n.*1899G>T
ENST00000637014.1:n.1938G>T
ENST00000637095.1:c.*1311G>T	ENSP00000490415.1:n.*1311G>T
ENST00000637244.1:c.*2049G>T	ENSP00000490188.1:n.*2049G>T
ENST00000637343.1:n.2968G>T
ENST00000637429.1:c.*1743G>T	ENSP00000490522.1:n.*1743G>T
ENST00000637484.1:c.*1493G>T	ENSP00000490837.1:n.*1493G>T
ENST00000637528.1:c.*343G>T	ENSP00000490801.1:n.*343G>T
ENST00000637609.1:n.4252G>T
ENST00000637636.1:c.*343G>T	ENSP00000490112.1:n.*343G>T
ENST00000637752.1:n.1973G>T
ENST00000637790.2:c.*343G>T MANE Select	ENSP00000490272.1:n.*343G>T
ENST00000637857.1:n.1897G>T
ENST00000637922.1:c.*343G>T	ENSP00000490071.1:n.*343G>T
ENST00000637991.1:c.*343G>T	ENSP00000489901.1:n.*343G>T
ENST00000638028.1:n.1748G>T
ENST00000638069.1:n.2352G>T
ENST00000262097.10:c.*343G>T	ENSP00000262097.6:n.*343G>T
ENST00000381733.8:c.*343G>T	ENSP00000371152.4:n.*343G>T
ENST00000520781.5:c.*343G>T	ENSP00000427751.1:n.*343G>T
NM_001127505.1:c.*343G>T	NP_001120977.1:n.*343G>T
NM_001127505.2:c.*343G>T	NP_001120977.1:n.*343G>T
NM_004315.4:c.*343G>T	NP_004306.3:n.*343G>T
NM_004315.5:c.*343G>T	NP_004306.3:n.*343G>T
NM_177924.3:c.*343G>T	NP_808592.2:n.*343G>T
NM_177924.4:c.*343G>T	NP_808592.2:n.*343G>T
XM_005273504.2:c.*343G>T	XP_005273561.1:n.*343G>T
NM_001363743.1:c.*343G>T	NP_001350672.1:n.*343G>T
XM_005273504.3:c.*343G>T	XP_005273561.1:n.*343G>T
NM_177924.5:c.*343G>T MANE Select	NP_808592.2:n.*343G>T
NM_001127505.3:c.*343G>T	NP_001120977.1:n.*343G>T
NM_001363743.2:c.*343G>T	NP_001350672.1:n.*343G>T
NM_004315.6:c.*343G>T	NP_004306.3:n.*343G>T