Canonical Allele Identifier: CA359203646

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13900328G>A , CM000667.2:g.13900328G>A	GRCh38
NC_000005.9:g.13900437G>A , CM000667.1:g.13900437G>A	GRCh37
NC_000005.8:g.13953437G>A	NCBI36
NG_013081.1:g.49153C>T
NG_013081.2:g.49153C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.2137C>T MANE Select	NP_001360.1:p.Gln713Ter
ENST00000265104.5:c.2137C>T MANE Select	ENSP00000265104.4:p.Gln713Ter
NM_001369.2:c.2137C>T	NP_001360.1:p.Gln713Ter
ENST00000265104.4:c.2137C>T	ENSP00000265104.4:p.Gln713Ter
ENST00000681290.1:c.2092C>T	ENSP00000505288.1:p.Gln698Ter
XM_005248262.2:c.2092C>T	XP_005248319.1:p.Gln698Ter
XM_005248262.3:c.2245C>T	XP_005248319.2:p.Gln749Ter
XM_011513990.1:c.2137C>T	XP_011512292.1:p.Gln713Ter
XM_017009177.1:c.2245C>T	XP_016864666.1:p.Gln749Ter
XM_017009178.1:c.1150C>T	XP_016864667.1:p.Gln384Ter
XM_017009179.2:c.1150C>T	XP_016864668.1:p.Gln384Ter
XM_017009180.1:c.2245C>T	XP_016864669.1:p.Gln749Ter
XM_017009181.1:c.2245C>T	XP_016864670.1:p.Gln749Ter
XM_017009182.1:c.2245C>T	XP_016864671.1:p.Gln749Ter
XM_017009183.1:c.2245C>T	XP_016864672.1:p.Gln749Ter
XM_017009184.1:c.2245C>T	XP_016864673.1:p.Gln749Ter
XM_017009187.1:c.2245C>T	XP_016864676.1:p.Gln749Ter
XM_024454388.1:c.1150C>T	XP_024310156.1:p.Gln384Ter
XM_024454389.1:c.739C>T	XP_024310157.1:p.Gln247Ter
XR_001742034.1:n.2262C>T
XR_001742035.1:n.2262C>T
XR_925598.1:n.2344C>T