Canonical Allele Identifier: CA1364839648

Gene: DNAH1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52396510G= , CM000665.2:g.52396510G=	GRCh38
NC_000003.11:g.52430526G= , CM000665.1:g.52430526G=	GRCh37
NC_000003.10:g.52405566G=	NCBI36
NG_052911.1:g.85192G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420323.7:c.11402G= MANE Select	ENSP00000401514.2:p.Gly3801=
ENST00000420323.6:c.11402G=	ENSP00000401514.2:p.Gly3801=
ENST00000486752.5:n.11859G=
ENST00000488988.5:n.3188G=
ENST00000490713.5:c.2102G=	ENSP00000419071.1:p.Gly701=
NM_015512.4:c.11402G=	NP_056327.4:p.Gly3801=
XM_011533577.1:c.11471G=	XP_011531879.1:p.Gly3824=
XM_017006129.1:c.11471G=	XP_016861618.1:p.Gly3824=
XM_017006130.1:c.11402G=	XP_016861619.1:p.Gly3801=
XM_017006131.1:c.11345G=	XP_016861620.1:p.Gly3782=
XR_001740098.1:n.14620G=
XR_001740099.1:n.14620G=
NM_015512.5:c.11402G= MANE Select	NP_056327.4:p.Gly3801=