Canonical Allele Identifier: CA2289322359

Gene: ABHD3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.21681471A= , CM000680.2:g.21681471A=	GRCh38
NC_000018.9:g.19261432A= , CM000680.1:g.19261432A=	GRCh37
NC_000018.8:g.17515430A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000289119.7:c.555+2449T= MANE Select	ENSP00000289119.2:n.555+2449T=
ENST00000289119.6:c.555+2449T=	ENSP00000289119.2:n.555+2449T=
ENST00000577891.1:c.*74+2449T=	ENSP00000463365.1:n.*74+2449T=
ENST00000578270.5:c.-471+2449T=	ENSP00000462578.1:n.-471+2449T=
ENST00000579875.5:n.485-17241T=
ENST00000580981.5:c.509+20845T=	ENSP00000462935.1:n.509+20845T=
NM_001308256.1:c.509+20845T=	NP_001295185.1:n.509+20845T=
NM_138340.4:c.555+2449T=	NP_612213.2:n.555+2449T=
XM_011525847.1:c.555+2449T=	XP_011524149.1:n.555+2449T=
XR_243847.1:n.695+2449T=
XR_935209.1:n.650-17241T=
XR_935210.1:n.650-17241T=
XM_011525847.3:c.555+2449T=	XP_011524149.1:n.555+2449T=
XM_017025572.1:c.-470-17241T=	XP_016881061.1:n.-470-17241T=
XM_017025573.1:c.-471+702T=	XP_016881062.1:n.-471+702T=
XM_017025574.1:c.-471+290T=	XP_016881063.1:n.-471+290T=
XM_024451094.1:c.-471+2449T=	XP_024306862.1:n.-471+2449T=
XR_001753151.2:n.683+2449T=
XR_002958165.1:n.683+2449T=
XR_935209.3:n.638-17241T=
XR_935210.3:n.638-17241T=
NM_138340.5:c.555+2449T= MANE Select	NP_612213.2:n.555+2449T=
NM_001308256.2:c.509+20845T=	NP_001295185.1:n.509+20845T=