Canonical Allele Identifier: CA1318502363

Gene: DNAH7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.195787230A= , CM000664.2:g.195787230A=	GRCh38
NC_000002.11:g.196651954A= , CM000664.1:g.196651954A=	GRCh37
NC_000002.10:g.196360199A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312428.11:c.10717-59T= MANE Select	ENSP00000311273.6:n.10717-59T=
ENST00000312428.10:c.10717-59T=	ENSP00000311273.6:n.10717-59T=
ENST00000409063.5:c.166-59T=	ENSP00000386912.1:n.166-59T=
NM_018897.2:c.10717-59T=	NP_061720.2:n.10717-59T=
XM_011511487.1:c.10717-59T=	XP_011509789.1:n.10717-59T=
XM_011511488.1:c.10597-59T=	XP_011509790.1:n.10597-59T=
XM_011511489.1:c.10579-59T=	XP_011509791.1:n.10579-59T=
XM_011511490.1:c.10492-59T=	XP_011509792.1:n.10492-59T=
XM_011511496.1:c.6361-59T=	XP_011509798.1:n.6361-59T=
XM_011511497.1:c.5089-59T=	XP_011509799.1:n.5089-59T=
XM_011511488.3:c.10597-59T=	XP_011509790.1:n.10597-59T=
XM_011511489.2:c.10579-59T=	XP_011509791.1:n.10579-59T=
XM_011511490.3:c.10492-59T=	XP_011509792.1:n.10492-59T=
XM_011511497.2:c.5089-59T=	XP_011509799.1:n.5089-59T=
XM_017004504.2:c.10444-59T=	XP_016859993.1:n.10444-59T=
NM_018897.3:c.10717-59T= MANE Select	NP_061720.2:n.10717-59T=