Canonical Allele Identifier: CA2580060522

Gene: DVL1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1339725C>T , CM000663.2:g.1339725C>T	GRCh38
NC_000001.10:g.1275105C>T , CM000663.1:g.1275105C>T	GRCh37
NC_000001.9:g.1264968C>T	NCBI36
NG_008048.1:g.14388G>A
NG_008048.2:g.14388G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001330311.2:c.986+11G>A MANE Select	NP_001317240.1:n.986+11G>A
ENST00000378888.10:c.986+11G>A MANE Select	ENSP00000368166.5:n.986+11G>A
NM_001330311.1:c.986+11G>A	NP_001317240.1:n.986+11G>A
NM_004421.2:c.986+11G>A	NP_004412.2:n.986+11G>A
NM_004421.3:c.986+11G>A	NP_004412.2:n.986+11G>A
ENST00000378888.9:c.986+11G>A	ENSP00000368166.5:n.986+11G>A
ENST00000378891.9:c.986+11G>A	ENSP00000368169.5:n.986+11G>A
ENST00000610709.2:c.650+734G>A	ENSP00000480077.1:n.650+734G>A
ENST00000631679.1:c.92+11G>A	ENSP00000488181.1:n.92+11G>A
ENST00000633096.1:n.347G>A
ENST00000634054.1:n.230+11G>A
XM_005244731.2:c.986+11G>A	XP_005244788.1:n.986+11G>A
XM_005244732.2:c.986+11G>A	XP_005244789.1:n.986+11G>A
XM_005244732.4:c.986+11G>A	XP_005244789.1:n.986+11G>A
XM_005244733.2:c.986+11G>A	XP_005244790.1:n.986+11G>A
XM_005244733.4:c.986+11G>A	XP_005244790.1:n.986+11G>A