Canonical Allele Identifier: CA684749086

Gene: DNAH10

Linked Data

• dbSNP Id: rs1182778075
• MyVariant Identifiers: chr12:g.124375233A>T (hg19) ; chr12:g.123890686A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123890686A>T , CM000674.2:g.123890686A>T	GRCh38
NC_000012.11:g.124375233A>T , CM000674.1:g.124375233A>T	GRCh37
NC_000012.10:g.122941186A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000409039.8:c.8825-2547A>T	ENSP00000386770.4:n.8825-2547A>T
ENST00000638045.1:c.8642-2547A>T	ENSP00000489675.1:n.8642-2547A>T
ENST00000673944.1:c.8996-2547A>T MANE Select	ENSP00000501095.1:n.8996-2547A>T
ENST00000409039.7:c.8642-2547A>T	ENSP00000386770.3:n.8642-2547A>T
NM_207437.3:c.8642-2547A>T	NP_997320.2:n.8642-2547A>T
XM_005253555.2:c.8996-2547A>T	XP_005253612.1:n.8996-2547A>T
XM_011538013.1:c.8987-2547A>T	XP_011536315.1:n.8987-2547A>T
XM_011538014.1:c.8837-2547A>T	XP_011536316.1:n.8837-2547A>T
XM_011538015.1:c.8807-2547A>T	XP_011536317.1:n.8807-2547A>T
XM_011538016.1:c.8807-2547A>T	XP_011536318.1:n.8807-2547A>T
XM_011538017.1:c.8660-2547A>T	XP_011536319.1:n.8660-2547A>T
XM_011538018.1:c.6512-2547A>T	XP_011536320.1:n.6512-2547A>T
XM_011538019.1:c.5837-2547A>T	XP_011536321.1:n.5837-2547A>T
XM_005253555.3:c.8996-2547A>T	XP_005253612.1:n.8996-2547A>T
XM_011538014.2:c.8837-2547A>T	XP_011536316.1:n.8837-2547A>T
XM_011538015.3:c.8807-2547A>T	XP_011536317.1:n.8807-2547A>T
XM_011538016.2:c.8807-2547A>T	XP_011536318.1:n.8807-2547A>T
XM_011538017.3:c.8660-2547A>T	XP_011536319.1:n.8660-2547A>T
XM_011538019.2:c.5837-2547A>T	XP_011536321.1:n.5837-2547A>T
XM_017018960.1:c.8995+3373A>T	XP_016874449.1:n.8995+3373A>T
XM_017018961.1:c.8687-2547A>T	XP_016874450.1:n.8687-2547A>T
XM_017018962.1:c.5756-2547A>T	XP_016874451.1:n.5756-2547A>T
XM_024448875.1:c.1244-2547A>T	XP_024304643.1:n.1244-2547A>T
NM_001372106.1:c.8996-2547A>T MANE Select	NP_001359035.1:n.8996-2547A>T