Canonical Allele Identifier: CA337862558

Gene: DVL1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1338378C>G , CM000663.2:g.1338378C>G	GRCh38
NC_000001.10:g.1273758C>G , CM000663.1:g.1273758C>G	GRCh37
NC_000001.9:g.1263621C>G	NCBI36
NG_008048.1:g.15735G>C
NG_008048.2:g.15735G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001330311.2:c.1398G>C MANE Select	NP_001317240.1:p.Glu466Asp
ENST00000378888.10:c.1398G>C MANE Select	ENSP00000368166.5:p.Glu466Asp
NM_001330311.1:c.1398G>C	NP_001317240.1:p.Glu466Asp
NM_004421.2:c.1323G>C	NP_004412.2:p.Glu441Asp
NM_004421.3:c.1323G>C	NP_004412.2:p.Glu441Asp
ENST00000378888.9:c.1398G>C	ENSP00000368166.5:p.Glu466Asp
ENST00000378891.9:c.1323G>C	ENSP00000368169.5:p.Glu441Asp
ENST00000610709.2:c.651-6G>C	ENSP00000480077.1:n.651-6G>C
ENST00000631679.1:c.429G>C	ENSP00000488181.1:p.Glu143Asp
ENST00000632445.1:c.327G>C	ENSP00000488888.1:p.Glu109Asp
ENST00000634054.1:n.784G>C
XM_005244731.2:c.1398G>C	XP_005244788.1:p.Glu466Asp
XM_005244732.2:c.1398G>C	XP_005244789.1:p.Glu466Asp
XM_005244732.4:c.1398G>C	XP_005244789.1:p.Glu466Asp
XM_005244733.2:c.1323G>C	XP_005244790.1:p.Glu441Asp
XM_005244733.4:c.1323G>C	XP_005244790.1:p.Glu441Asp