Canonical Allele Identifier: CA2341406
Community Standard Title: NM_016006.6(ABHD5):c.662-10T>G
Gene: ABHD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.43714937T>G , CM000665.2:g.43714937T>G GRCh38
NC_000003.11:g.43756429T>G , CM000665.1:g.43756429T>G GRCh37
NC_000003.10:g.43731433T>G NCBI36
NG_007090.3:g.29055T>G
NG_007090.5:g.29068T>G

Transcript Alleles

HGVS Amino-acid Change
NM_016006.6:c.662-10T>G MANE Select NP_057090.2:n.662-10T>G
ENST00000644371.2:c.662-10T>G MANE Select ENSP00000495778.1:n.662-10T>G
NM_001355186.1:c.662-10T>G NP_001342115.1:n.662-10T>G
NM_001355186.2:c.662-10T>G NP_001342115.1:n.662-10T>G
NM_001365649.1:c.539-10T>G NP_001352578.1:n.539-10T>G
NM_001365650.1:c.662-10T>G NP_001352579.1:n.662-10T>G
NM_016006.4:c.662-10T>G NP_057090.2:n.662-10T>G
NM_016006.5:c.662-10T>G NP_057090.2:n.662-10T>G
NR_158560.1:n.785-2734T>G
ENST00000013894.3:c.*656-10T>G ENSP00000013894.2:n.*656-10T>G
ENST00000413300.1:c.158-10T>G ENSP00000392159.1:n.158-10T>G
ENST00000413300.2:c.156-10T>G
ENST00000454293.2:c.539-10T>G ENSP00000412014.2:n.539-10T>G
ENST00000458276.6:c.662-10T>G ENSP00000390849.2:n.662-10T>G
ENST00000458276.7:c.662-10T>G ENSP00000390849.3:n.662-10T>G
ENST00000642351.1:c.539-10T>G ENSP00000494478.1:n.539-10T>G
ENST00000643140.1:c.*136-2734T>G ENSP00000495588.1:n.*136-2734T>G
ENST00000643477.1:c.*235-2734T>G ENSP00000496220.1:n.*235-2734T>G
ENST00000643500.1:c.662-2734T>G ENSP00000494735.1:n.662-2734T>G
ENST00000643520.1:n.828-10T>G
ENST00000646378.1:c.*712-10T>G ENSP00000495826.1:n.*712-10T>G
ENST00000646799.1:c.*136-10T>G ENSP00000494829.1:n.*136-10T>G
ENST00000649763.1:c.662-10T>G ENSP00000497701.1:n.662-10T>G
XM_011533779.1:c.539-10T>G XP_011532081.1:n.539-10T>G
XM_011533780.1:c.662-10T>G XP_011532082.1:n.662-10T>G
XR_940447.1:n.719-2734T>G