Canonical Allele Identifier: CA1360918344
Gene: ABHD5 HGNC NCBI

Linked Data

dbSNP Id: rs2084821544

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.43720493C>T , CM000665.2:g.43720493C>T GRCh38
NC_000003.11:g.43761985C>T , CM000665.1:g.43761985C>T GRCh37
NC_000003.10:g.43736989C>T NCBI36
NG_007090.3:g.34611C>T
NG_007090.5:g.34624C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000454293.2:c.*29+1932C>T ENSP00000412014.2:n.*29+1932C>T
ENST00000463153.2:c.306+1932C>T
ENST00000643477.1:c.*2472C>T ENSP00000496220.1:n.*2472C>T
ENST00000644371.2:c.*1961C>T MANE Select ENSP00000495778.1:n.*1961C>T
ENST00000649763.1:c.*29+1932C>T ENSP00000497701.1:n.*29+1932C>T
ENST00000463153.1:n.309+1932C>T
NM_016006.4:c.*1961C>T NP_057090.2:n.*1961C>T
XM_011533779.1:c.*1961C>T XP_011532081.1:n.*1961C>T
XM_011533780.1:c.*1987C>T XP_011532082.1:n.*1987C>T
XR_940447.1:n.2956C>T
NM_001355186.1:c.*29+1932C>T NP_001342115.1:n.*29+1932C>T
NM_001365649.1:c.*1961C>T NP_001352578.1:n.*1961C>T
NM_001365650.1:c.*1987C>T NP_001352579.1:n.*1987C>T
NM_016006.5:c.*1961C>T NP_057090.2:n.*1961C>T
NR_158560.1:n.3022C>T
NM_001355186.2:c.*29+1932C>T NP_001342115.1:n.*29+1932C>T
NM_016006.6:c.*1961C>T MANE Select NP_057090.2:n.*1961C>T