Canonical Allele Identifier: CA337857296

Gene: DVL1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1336516C>T , CM000663.2:g.1336516C>T	GRCh38
NC_000001.10:g.1271896C>T , CM000663.1:g.1271896C>T	GRCh37
NC_000001.9:g.1261759C>T	NCBI36
NG_008048.1:g.17597G>A
NG_008048.2:g.17597G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001330311.2:c.1715-1G>A MANE Select	NP_001317240.1:n.1715-1G>A
ENST00000378888.10:c.1715-1G>A MANE Select	ENSP00000368166.5:n.1715-1G>A
NM_001330311.1:c.1715-1G>A	NP_001317240.1:n.1715-1G>A
NM_004421.2:c.1640-1G>A	NP_004412.2:n.1640-1G>A
NM_004421.3:c.1640-1G>A	NP_004412.2:n.1640-1G>A
ENST00000378888.9:c.1715-1G>A	ENSP00000368166.5:n.1715-1G>A
ENST00000378891.9:c.1640-1G>A	ENSP00000368169.5:n.1640-1G>A
ENST00000610709.2:c.962-1G>A	ENSP00000480077.1:n.962-1G>A
ENST00000632445.1:c.682-1G>A	ENSP00000488888.1:n.682-1G>A
XM_005244731.2:c.1715-1G>A	XP_005244788.1:n.1715-1G>A
XM_005244732.2:c.*28-1G>A	XP_005244789.1:n.*28-1G>A
XM_005244732.4:c.*28-1G>A	XP_005244789.1:n.*28-1G>A
XM_005244733.2:c.*28-1G>A	XP_005244790.1:n.*28-1G>A
XM_005244733.4:c.*28-1G>A	XP_005244790.1:n.*28-1G>A