Canonical Allele Identifier: CA1360917225
Gene: ABHD5 HGNC NCBI

Linked Data

dbSNP Id: rs2084787867

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.43717915C>T , CM000665.2:g.43717915C>T GRCh38
NC_000003.11:g.43759407C>T , CM000665.1:g.43759407C>T GRCh37
NC_000003.10:g.43734411C>T NCBI36
NG_007090.3:g.32033C>T
NG_007090.5:g.32046C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000413300.2:c.359+58C>T
ENST00000454293.2:c.837+58C>T ENSP00000412014.2:n.837+58C>T
ENST00000458276.7:c.774-528C>T ENSP00000390849.3:n.774-528C>T
ENST00000463153.2:c.187+58C>T
ENST00000642351.1:c.837+58C>T ENSP00000494478.1:n.837+58C>T
ENST00000643140.1:c.*322+58C>T ENSP00000495588.1:n.*322+58C>T
ENST00000643477.1:c.*421+58C>T ENSP00000496220.1:n.*421+58C>T
ENST00000643500.1:c.*161+58C>T ENSP00000494735.1:n.*161+58C>T
ENST00000643520.1:n.1126+58C>T
ENST00000644371.2:c.960+58C>T MANE Select ENSP00000495778.1:n.960+58C>T
ENST00000646378.1:c.*1010+58C>T ENSP00000495826.1:n.*1010+58C>T
ENST00000646799.1:c.*248-528C>T ENSP00000494829.1:n.*248-528C>T
ENST00000649763.1:c.960+58C>T ENSP00000497701.1:n.960+58C>T
ENST00000413300.1:c.361+58C>T ENSP00000392159.1:n.361+58C>T
ENST00000458276.6:c.960+58C>T ENSP00000390849.2:n.960+58C>T
ENST00000463153.1:n.190+58C>T
NM_016006.4:c.960+58C>T NP_057090.2:n.960+58C>T
XM_011533779.1:c.837+58C>T XP_011532081.1:n.837+58C>T
XM_011533780.1:c.774-528C>T XP_011532082.1:n.774-528C>T
XR_940447.1:n.905+58C>T
NM_001355186.1:c.960+58C>T NP_001342115.1:n.960+58C>T
NM_001365649.1:c.837+58C>T NP_001352578.1:n.837+58C>T
NM_001365650.1:c.774-528C>T NP_001352579.1:n.774-528C>T
NM_016006.5:c.960+58C>T NP_057090.2:n.960+58C>T
NR_158560.1:n.971+58C>T
NM_001355186.2:c.960+58C>T NP_001342115.1:n.960+58C>T
NM_016006.6:c.960+58C>T MANE Select NP_057090.2:n.960+58C>T