Canonical Allele Identifier: CA13730840

Gene: DNAH10

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123832329A>G , CM000674.2:g.123832329A>G	GRCh38
NC_000012.11:g.124316876A>G , CM000674.1:g.124316876A>G	GRCh37
NC_000012.10:g.122882829A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409039.8:c.4375-785A>G	ENSP00000386770.4:n.4375-785A>G
ENST00000638045.1:c.4192-785A>G	ENSP00000489675.1:n.4192-785A>G
ENST00000673944.1:c.4546-785A>G MANE Select	ENSP00000501095.1:n.4546-785A>G
ENST00000409039.7:c.4192-785A>G	ENSP00000386770.3:n.4192-785A>G
NM_207437.3:c.4192-785A>G	NP_997320.2:n.4192-785A>G
XM_005253555.2:c.4546-785A>G	XP_005253612.1:n.4546-785A>G
XM_011538013.1:c.4546-785A>G	XP_011536315.1:n.4546-785A>G
XM_011538014.1:c.4546-785A>G	XP_011536316.1:n.4546-785A>G
XM_011538015.1:c.4546-785A>G	XP_011536317.1:n.4546-785A>G
XM_011538016.1:c.4546-785A>G	XP_011536318.1:n.4546-785A>G
XM_011538017.1:c.4546-785A>G	XP_011536319.1:n.4546-785A>G
XM_011538018.1:c.2062-785A>G	XP_011536320.1:n.2062-785A>G
XM_011538019.1:c.1387-785A>G	XP_011536321.1:n.1387-785A>G
XM_011538020.1:c.4546-785A>G	XP_011536322.1:n.4546-785A>G
XM_005253555.3:c.4546-785A>G	XP_005253612.1:n.4546-785A>G
XM_011538014.2:c.4546-785A>G	XP_011536316.1:n.4546-785A>G
XM_011538015.3:c.4546-785A>G	XP_011536317.1:n.4546-785A>G
XM_011538016.2:c.4546-785A>G	XP_011536318.1:n.4546-785A>G
XM_011538017.3:c.4546-785A>G	XP_011536319.1:n.4546-785A>G
XM_011538019.2:c.1387-785A>G	XP_011536321.1:n.1387-785A>G
XM_011538020.2:c.4546-785A>G	XP_011536322.1:n.4546-785A>G
XM_017018960.1:c.4546-785A>G	XP_016874449.1:n.4546-785A>G
XM_017018961.1:c.4237-785A>G	XP_016874450.1:n.4237-785A>G
XM_017018962.1:c.1306-785A>G	XP_016874451.1:n.1306-785A>G
NM_001372106.1:c.4546-785A>G MANE Select	NP_001359035.1:n.4546-785A>G