Canonical Allele Identifier: CA359209052

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13840957G>C , CM000667.2:g.13840957G>C	GRCh38
NC_000005.9:g.13841066G>C , CM000667.1:g.13841066G>C	GRCh37
NC_000005.8:g.13894066G>C	NCBI36
NG_013081.1:g.108524C>G
NG_013081.2:g.108524C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.5658C>G MANE Select	NP_001360.1:p.Tyr1886Ter
ENST00000265104.5:c.5658C>G MANE Select	ENSP00000265104.4:p.Tyr1886Ter
NM_001369.2:c.5658C>G	NP_001360.1:p.Tyr1886Ter
ENST00000265104.4:c.5658C>G	ENSP00000265104.4:p.Tyr1886Ter
ENST00000681290.1:c.5613C>G	ENSP00000505288.1:p.Tyr1871Ter
XM_005248262.2:c.5613C>G	XP_005248319.1:p.Tyr1871Ter
XM_005248262.3:c.5766C>G	XP_005248319.2:p.Tyr1922Ter
XM_011513990.1:c.5658C>G	XP_011512292.1:p.Tyr1886Ter
XM_017009177.1:c.5766C>G	XP_016864666.1:p.Tyr1922Ter
XM_017009178.1:c.4671C>G	XP_016864667.1:p.Tyr1557Ter
XM_017009179.2:c.4671C>G	XP_016864668.1:p.Tyr1557Ter
XM_017009180.1:c.5766C>G	XP_016864669.1:p.Tyr1922Ter
XM_017009181.1:c.5766C>G	XP_016864670.1:p.Tyr1922Ter
XM_017009182.1:c.5766C>G	XP_016864671.1:p.Tyr1922Ter
XM_017009183.1:c.5766C>G	XP_016864672.1:p.Tyr1922Ter
XM_017009184.1:c.5766C>G	XP_016864673.1:p.Tyr1922Ter
XM_017009185.1:c.855C>G	XP_016864674.1:p.Tyr285Ter
XM_017009186.1:c.408C>G	XP_016864675.1:p.Tyr136Ter
XM_017009187.1:c.5766C>G	XP_016864676.1:p.Tyr1922Ter
XM_024454388.1:c.4671C>G	XP_024310156.1:p.Tyr1557Ter
XM_024454389.1:c.4260C>G	XP_024310157.1:p.Tyr1420Ter
XR_001742034.1:n.5783C>G
XR_001742035.1:n.5783C>G
XR_925598.1:n.5865C>G