Canonical Allele Identifier: CA4101958

Gene: DACT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.168319600C>T , CM000668.2:g.168319600C>T	GRCh38
NC_000006.11:g.168720280C>T , CM000668.1:g.168720280C>T	GRCh37
NC_000006.10:g.168463129C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_214462.5:c.34G>A MANE Select	NP_999627.2:p.Gly12Ser
ENST00000366795.4:c.34G>A MANE Select	ENSP00000355760.3:p.Gly12Ser
NM_001286350.1:c.-8+54G>A	NP_001273279.1:n.-8+54G>A
NM_001286350.2:c.-8+54G>A	NP_001273279.1:n.-8+54G>A
NM_001286351.1:c.34G>A	NP_001273280.1:p.Gly12Ser
NM_001286351.2:c.34G>A	NP_001273280.1:p.Gly12Ser
NM_214462.4:c.34G>A	NP_999627.2:p.Gly12Ser
NR_104425.1:n.155G>A
NR_104425.2:n.178G>A
ENST00000366795.3:c.34G>A	ENSP00000355760.3:p.Gly12Ser
ENST00000366796.7:c.34G>A	ENSP00000355761.2:p.Gly12Ser
ENST00000607983.1:c.-200G>A	ENSP00000476434.1:n.-200G>A
ENST00000610183.1:c.-8+54G>A	ENSP00000476573.1:n.-8+54G>A