Canonical Allele Identifier: CA1318502140

Gene: DNAH7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.195787145G= , CM000664.2:g.195787145G=	GRCh38
NC_000002.11:g.196651869G= , CM000664.1:g.196651869G=	GRCh37
NC_000002.10:g.196360114G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312428.11:c.10743C= MANE Select	ENSP00000311273.6:p.Gly3581=
ENST00000312428.10:c.10743C=	ENSP00000311273.6:p.Gly3581=
ENST00000409063.5:c.192C=	ENSP00000386912.1:p.Gly64=
NM_018897.2:c.10743C=	NP_061720.2:p.Gly3581=
XM_011511487.1:c.10743C=	XP_011509789.1:p.Gly3581=
XM_011511488.1:c.10623C=	XP_011509790.1:p.Gly3541=
XM_011511489.1:c.10605C=	XP_011509791.1:p.Gly3535=
XM_011511490.1:c.10518C=	XP_011509792.1:p.Gly3506=
XM_011511496.1:c.6387C=	XP_011509798.1:p.Gly2129=
XM_011511497.1:c.5115C=	XP_011509799.1:p.Gly1705=
XM_011511488.3:c.10623C=	XP_011509790.1:p.Gly3541=
XM_011511489.2:c.10605C=	XP_011509791.1:p.Gly3535=
XM_011511490.3:c.10518C=	XP_011509792.1:p.Gly3506=
XM_011511497.2:c.5115C=	XP_011509799.1:p.Gly1705=
XM_017004504.2:c.10470C=	XP_016859993.1:p.Gly3490=
NM_018897.3:c.10743C= MANE Select	NP_061720.2:p.Gly3581=