Canonical Allele Identifier: CA1318501909

Gene: DNAH7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.195787080G= , CM000664.2:g.195787080G=	GRCh38
NC_000002.11:g.196651804G= , CM000664.1:g.196651804G=	GRCh37
NC_000002.10:g.196360049G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312428.11:c.10808C= MANE Select	ENSP00000311273.6:p.Pro3603=
ENST00000312428.10:c.10808C=	ENSP00000311273.6:p.Pro3603=
ENST00000409063.5:c.257C=	ENSP00000386912.1:p.Pro86=
NM_018897.2:c.10808C=	NP_061720.2:p.Pro3603=
XM_011511487.1:c.10808C=	XP_011509789.1:p.Pro3603=
XM_011511488.1:c.10688C=	XP_011509790.1:p.Pro3563=
XM_011511489.1:c.10670C=	XP_011509791.1:p.Pro3557=
XM_011511490.1:c.10583C=	XP_011509792.1:p.Pro3528=
XM_011511496.1:c.6452C=	XP_011509798.1:p.Pro2151=
XM_011511497.1:c.5180C=	XP_011509799.1:p.Pro1727=
XM_011511488.3:c.10688C=	XP_011509790.1:p.Pro3563=
XM_011511489.2:c.10670C=	XP_011509791.1:p.Pro3557=
XM_011511490.3:c.10583C=	XP_011509792.1:p.Pro3528=
XM_011511497.2:c.5180C=	XP_011509799.1:p.Pro1727=
XM_017004504.2:c.10535C=	XP_016859993.1:p.Pro3512=
NM_018897.3:c.10808C= MANE Select	NP_061720.2:p.Pro3603=