Canonical Allele Identifier: CA1425890203

Gene: DVL3 EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184158724A= , CM000665.2:g.184158724A=	GRCh38
NC_000003.11:g.183876512A= , CM000665.1:g.183876512A=	GRCh37
NC_000003.10:g.185359206A=	NCBI36
NG_046860.1:g.8414A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313143.9:c.161+2928A= (DVL3) MANE Select	ENSP00000316054.3:n.161+2928A=
ENST00000431765.6:c.161+2928A= (DVL3)	ENSP00000405885.1:n.161+2928A=
ENST00000435708.6:c.*15+2277A= (DVL3)	ENSP00000412345.1:n.*15+2277A=
ENST00000649364.1:c.161+2928A= (DVL3)	ENSP00000497340.1:n.161+2928A=
ENST00000313143.7:c.161+2928A= (DVL3)	ENSP00000316054.3:n.161+2928A=
ENST00000423300.1:c.-146+1657A= (DVL3)	ENSP00000393849.1:n.-146+1657A=
ENST00000431765.5:c.161+2928A= (DVL3)	ENSP00000405885.1:n.161+2928A=
ENST00000435708.5:c.*15+2277A= (DVL3)	ENSP00000412345.1:n.*15+2277A=
ENST00000444495.1:c.2106+14017A= (EIF2B5)	ENSP00000409142.1:n.2106+14017A=
ENST00000462665.5:n.235+2928A= (DVL3)
NM_004423.3:c.161+2928A= (DVL3)	NP_004414.3:n.161+2928A=
XM_005247172.1:c.161+2928A= (DVL3)	XP_005247229.1:n.161+2928A=
NM_004423.4:c.161+2928A= (DVL3) MANE Select	NP_004414.3:n.161+2928A=
XM_005247172.2:c.161+2928A= (DVL3)	XP_005247229.1:n.161+2928A=