Canonical Allele Identifier: CA3204447

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13885021C>T , CM000667.2:g.13885021C>T	GRCh38
NC_000005.9:g.13885130C>T , CM000667.1:g.13885130C>T	GRCh37
NC_000005.8:g.13938130C>T	NCBI36
NG_013081.1:g.64460G>A
NG_013081.2:g.64460G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.2951G>A MANE Select	NP_001360.1:p.Arg984His
ENST00000265104.5:c.2951G>A MANE Select	ENSP00000265104.4:p.Arg984His
NM_001369.2:c.2951G>A	NP_001360.1:p.Arg984His
ENST00000265104.4:c.2951G>A	ENSP00000265104.4:p.Arg984His
ENST00000681290.1:c.2906G>A	ENSP00000505288.1:p.Arg969His
XM_005248262.2:c.2906G>A	XP_005248319.1:p.Arg969His
XM_005248262.3:c.3059G>A	XP_005248319.2:p.Arg1020His
XM_011513990.1:c.2951G>A	XP_011512292.1:p.Arg984His
XM_017009177.1:c.3059G>A	XP_016864666.1:p.Arg1020His
XM_017009178.1:c.1964G>A	XP_016864667.1:p.Arg655His
XM_017009179.2:c.1964G>A	XP_016864668.1:p.Arg655His
XM_017009180.1:c.3059G>A	XP_016864669.1:p.Arg1020His
XM_017009181.1:c.3059G>A	XP_016864670.1:p.Arg1020His
XM_017009182.1:c.3059G>A	XP_016864671.1:p.Arg1020His
XM_017009183.1:c.3059G>A	XP_016864672.1:p.Arg1020His
XM_017009184.1:c.3059G>A	XP_016864673.1:p.Arg1020His
XM_017009187.1:c.3059G>A	XP_016864676.1:p.Arg1020His
XM_024454388.1:c.1964G>A	XP_024310156.1:p.Arg655His
XM_024454389.1:c.1553G>A	XP_024310157.1:p.Arg518His
XR_001742034.1:n.3076G>A
XR_001742035.1:n.3076G>A
XR_925598.1:n.3158G>A