Canonical Allele Identifier: CA433761183

Gene: DNAH1

Linked Data

• MyVariant Identifiers: chr3:g.52387625T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52353609T>G , CM000665.2:g.52353609T>G	GRCh38
NC_000003.11:g.52387625T>G , CM000665.1:g.52387625T>G	GRCh37
NC_000003.10:g.52362665T>G	NCBI36
NG_052911.1:g.42291T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420323.7:c.3456T>G MANE Select	ENSP00000401514.2:p.Ala1152=
ENST00000420323.6:c.3456T>G	ENSP00000401514.2:p.Ala1152=
ENST00000486752.5:n.3717T>G
ENST00000497875.1:n.3621T>G
NM_015512.4:c.3456T>G	NP_056327.4:p.Ala1152=
XM_011533577.1:c.3456T>G	XP_011531879.1:p.Ala1152=
XM_017006129.1:c.3456T>G	XP_016861618.1:p.Ala1152=
XM_017006130.1:c.3456T>G	XP_016861619.1:p.Ala1152=
XM_017006131.1:c.3456T>G	XP_016861620.1:p.Ala1152=
XM_017006132.1:c.3456T>G	XP_016861621.1:p.Ala1152=
XM_017006133.1:c.3456T>G	XP_016861622.1:p.Ala1152=
XR_001740098.1:n.6605T>G
XR_001740099.1:n.6605T>G
NM_015512.5:c.3456T>G MANE Select	NP_056327.4:p.Ala1152=