Canonical Allele Identifier: CA1528441873

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13794042T= , CM000667.2:g.13794042T=	GRCh38
NC_000005.9:g.13794151T= , CM000667.1:g.13794151T=	GRCh37
NC_000005.8:g.13847151T=	NCBI36
NG_013081.1:g.155439A=
NG_013081.2:g.155439A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.7904A= MANE Select	ENSP00000265104.4:p.Tyr2635=
ENST00000681290.1:c.7859A=	ENSP00000505288.1:p.Tyr2620=
ENST00000265104.4:c.7904A=	ENSP00000265104.4:p.Tyr2635=
NM_001369.2:c.7904A=	NP_001360.1:p.Tyr2635=
XM_005248262.2:c.7859A=	XP_005248319.1:p.Tyr2620=
XM_011513990.1:c.7904A=	XP_011512292.1:p.Tyr2635=
XR_925598.1:n.8111A=
XM_005248262.3:c.8012A=	XP_005248319.2:p.Tyr2671=
XM_017009177.1:c.8012A=	XP_016864666.1:p.Tyr2671=
XM_017009178.1:c.6917A=	XP_016864667.1:p.Tyr2306=
XM_017009179.2:c.6917A=	XP_016864668.1:p.Tyr2306=
XM_017009180.1:c.8012A=	XP_016864669.1:p.Tyr2671=
XM_017009181.1:c.8012A=	XP_016864670.1:p.Tyr2671=
XM_017009182.1:c.8012A=	XP_016864671.1:p.Tyr2671=
XM_017009183.1:c.8012A=	XP_016864672.1:p.Tyr2671=
XM_017009184.1:c.8012A=	XP_016864673.1:p.Tyr2671=
XM_017009185.1:c.3101A=	XP_016864674.1:p.Tyr1034=
XM_017009186.1:c.2654A=	XP_016864675.1:p.Tyr885=
XM_017009187.1:c.*7A=	XP_016864676.1:n.*7A=
XM_017009188.1:c.1991A=	XP_016864677.1:p.Tyr664=
XM_024454388.1:c.6917A=	XP_024310156.1:p.Tyr2306=
XM_024454389.1:c.6506A=	XP_024310157.1:p.Tyr2169=
XR_001742034.1:n.8029A=
XR_001742035.1:n.8029A=
NM_001369.3:c.7904A= MANE Select	NP_001360.1:p.Tyr2635=