Canonical Allele Identifier: CA2289322364

Gene: ABHD3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.21681479G= , CM000680.2:g.21681479G=	GRCh38
NC_000018.9:g.19261440G= , CM000680.1:g.19261440G=	GRCh37
NC_000018.8:g.17515438G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000289119.7:c.555+2441C= MANE Select	ENSP00000289119.2:n.555+2441C=
ENST00000289119.6:c.555+2441C=	ENSP00000289119.2:n.555+2441C=
ENST00000577891.1:c.*74+2441C=	ENSP00000463365.1:n.*74+2441C=
ENST00000578270.5:c.-471+2441C=	ENSP00000462578.1:n.-471+2441C=
ENST00000579875.5:n.485-17249C=
ENST00000580981.5:c.509+20837C=	ENSP00000462935.1:n.509+20837C=
NM_001308256.1:c.509+20837C=	NP_001295185.1:n.509+20837C=
NM_138340.4:c.555+2441C=	NP_612213.2:n.555+2441C=
XM_011525847.1:c.555+2441C=	XP_011524149.1:n.555+2441C=
XR_243847.1:n.695+2441C=
XR_935209.1:n.650-17249C=
XR_935210.1:n.650-17249C=
XM_011525847.3:c.555+2441C=	XP_011524149.1:n.555+2441C=
XM_017025572.1:c.-470-17249C=	XP_016881061.1:n.-470-17249C=
XM_017025573.1:c.-471+694C=	XP_016881062.1:n.-471+694C=
XM_017025574.1:c.-471+282C=	XP_016881063.1:n.-471+282C=
XM_024451094.1:c.-471+2441C=	XP_024306862.1:n.-471+2441C=
XR_001753151.2:n.683+2441C=
XR_002958165.1:n.683+2441C=
XR_935209.3:n.638-17249C=
XR_935210.3:n.638-17249C=
NM_138340.5:c.555+2441C= MANE Select	NP_612213.2:n.555+2441C=
NM_001308256.2:c.509+20837C=	NP_001295185.1:n.509+20837C=