Canonical Allele Identifier: CA2289322339
Gene: ABHD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.21681435C= , CM000680.2:g.21681435C= GRCh38
NC_000018.9:g.19261396C= , CM000680.1:g.19261396C= GRCh37
NC_000018.8:g.17515394C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000289119.7:c.555+2485G= MANE Select ENSP00000289119.2:n.555+2485G=
ENST00000289119.6:c.555+2485G= ENSP00000289119.2:n.555+2485G=
ENST00000577891.1:c.*74+2485G= ENSP00000463365.1:n.*74+2485G=
ENST00000578270.5:c.-471+2485G= ENSP00000462578.1:n.-471+2485G=
ENST00000579875.5:n.485-17205G=
ENST00000580981.5:c.509+20881G= ENSP00000462935.1:n.509+20881G=
NM_001308256.1:c.509+20881G= NP_001295185.1:n.509+20881G=
NM_138340.4:c.555+2485G= NP_612213.2:n.555+2485G=
XM_011525847.1:c.555+2485G= XP_011524149.1:n.555+2485G=
XR_243847.1:n.695+2485G=
XR_935209.1:n.650-17205G=
XR_935210.1:n.650-17205G=
XM_011525847.3:c.555+2485G= XP_011524149.1:n.555+2485G=
XM_017025572.1:c.-470-17205G= XP_016881061.1:n.-470-17205G=
XM_017025573.1:c.-471+738G= XP_016881062.1:n.-471+738G=
XM_017025574.1:c.-471+326G= XP_016881063.1:n.-471+326G=
XM_024451094.1:c.-471+2485G= XP_024306862.1:n.-471+2485G=
XR_001753151.2:n.683+2485G=
XR_002958165.1:n.683+2485G=
XR_935209.3:n.638-17205G=
XR_935210.3:n.638-17205G=
NM_138340.5:c.555+2485G= MANE Select NP_612213.2:n.555+2485G=
NM_001308256.2:c.509+20881G= NP_001295185.1:n.509+20881G=