Canonical Allele Identifier: CA2069071552

Gene: DNAH10

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123890695A= , CM000674.2:g.123890695A=	GRCh38
NC_000012.11:g.124375242A= , CM000674.1:g.124375242A=	GRCh37
NC_000012.10:g.122941195A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000409039.8:c.8825-2538A=	ENSP00000386770.4:n.8825-2538A=
ENST00000638045.1:c.8642-2538A=	ENSP00000489675.1:n.8642-2538A=
ENST00000673944.1:c.8996-2538A= MANE Select	ENSP00000501095.1:n.8996-2538A=
ENST00000409039.7:c.8642-2538A=	ENSP00000386770.3:n.8642-2538A=
NM_207437.3:c.8642-2538A=	NP_997320.2:n.8642-2538A=
XM_005253555.2:c.8996-2538A=	XP_005253612.1:n.8996-2538A=
XM_011538013.1:c.8987-2538A=	XP_011536315.1:n.8987-2538A=
XM_011538014.1:c.8837-2538A=	XP_011536316.1:n.8837-2538A=
XM_011538015.1:c.8807-2538A=	XP_011536317.1:n.8807-2538A=
XM_011538016.1:c.8807-2538A=	XP_011536318.1:n.8807-2538A=
XM_011538017.1:c.8660-2538A=	XP_011536319.1:n.8660-2538A=
XM_011538018.1:c.6512-2538A=	XP_011536320.1:n.6512-2538A=
XM_011538019.1:c.5837-2538A=	XP_011536321.1:n.5837-2538A=
XM_005253555.3:c.8996-2538A=	XP_005253612.1:n.8996-2538A=
XM_011538014.2:c.8837-2538A=	XP_011536316.1:n.8837-2538A=
XM_011538015.3:c.8807-2538A=	XP_011536317.1:n.8807-2538A=
XM_011538016.2:c.8807-2538A=	XP_011536318.1:n.8807-2538A=
XM_011538017.3:c.8660-2538A=	XP_011536319.1:n.8660-2538A=
XM_011538019.2:c.5837-2538A=	XP_011536321.1:n.5837-2538A=
XM_017018960.1:c.8995+3382A=	XP_016874449.1:n.8995+3382A=
XM_017018961.1:c.8687-2538A=	XP_016874450.1:n.8687-2538A=
XM_017018962.1:c.5756-2538A=	XP_016874451.1:n.5756-2538A=
XM_024448875.1:c.1244-2538A=	XP_024304643.1:n.1244-2538A=
NM_001372106.1:c.8996-2538A= MANE Select	NP_001359035.1:n.8996-2538A=