Canonical Allele Identifier: CA359200474

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13829693A>C , CM000667.2:g.13829693A>C	GRCh38
NC_000005.9:g.13829802A>C , CM000667.1:g.13829802A>C	GRCh37
NC_000005.8:g.13882802A>C	NCBI36
NG_013081.1:g.119788T>G
NG_013081.2:g.119788T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.6261T>G MANE Select	NP_001360.1:p.Tyr2087Ter
ENST00000265104.5:c.6261T>G MANE Select	ENSP00000265104.4:p.Tyr2087Ter
NM_001369.2:c.6261T>G	NP_001360.1:p.Tyr2087Ter
ENST00000265104.4:c.6261T>G	ENSP00000265104.4:p.Tyr2087Ter
ENST00000681290.1:c.6216T>G	ENSP00000505288.1:p.Tyr2072Ter
ENST00000683090.1:n.1192T>G
XM_005248262.2:c.6216T>G	XP_005248319.1:p.Tyr2072Ter
XM_005248262.3:c.6369T>G	XP_005248319.2:p.Tyr2123Ter
XM_011513990.1:c.6261T>G	XP_011512292.1:p.Tyr2087Ter
XM_017009177.1:c.6369T>G	XP_016864666.1:p.Tyr2123Ter
XM_017009178.1:c.5274T>G	XP_016864667.1:p.Tyr1758Ter
XM_017009179.2:c.5274T>G	XP_016864668.1:p.Tyr1758Ter
XM_017009180.1:c.6369T>G	XP_016864669.1:p.Tyr2123Ter
XM_017009181.1:c.6369T>G	XP_016864670.1:p.Tyr2123Ter
XM_017009182.1:c.6369T>G	XP_016864671.1:p.Tyr2123Ter
XM_017009183.1:c.6369T>G	XP_016864672.1:p.Tyr2123Ter
XM_017009184.1:c.6369T>G	XP_016864673.1:p.Tyr2123Ter
XM_017009185.1:c.1458T>G	XP_016864674.1:p.Tyr486Ter
XM_017009186.1:c.1011T>G	XP_016864675.1:p.Tyr337Ter
XM_017009187.1:c.6369T>G	XP_016864676.1:p.Tyr2123Ter
XM_017009188.1:c.348T>G	XP_016864677.1:p.Tyr116Ter
XM_024454388.1:c.5274T>G	XP_024310156.1:p.Tyr1758Ter
XM_024454389.1:c.4863T>G	XP_024310157.1:p.Tyr1621Ter
XR_001742034.1:n.6386T>G
XR_001742035.1:n.6386T>G
XR_925598.1:n.6468T>G