Canonical Allele Identifier: CA1528476304

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13866254G= , CM000667.2:g.13866254G=	GRCh38
NC_000005.9:g.13866363G= , CM000667.1:g.13866363G=	GRCh37
NC_000005.8:g.13919363G=	NCBI36
NG_013081.1:g.83227C=
NG_013081.2:g.83227C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.4082C= MANE Select	ENSP00000265104.4:p.Pro1361=
ENST00000681290.1:c.4037C=	ENSP00000505288.1:p.Pro1346=
ENST00000265104.4:c.4082C=	ENSP00000265104.4:p.Pro1361=
NM_001369.2:c.4082C=	NP_001360.1:p.Pro1361=
XM_005248262.2:c.4037C=	XP_005248319.1:p.Pro1346=
XM_011513990.1:c.4082C=	XP_011512292.1:p.Pro1361=
XR_925598.1:n.4289C=
XM_005248262.3:c.4190C=	XP_005248319.2:p.Pro1397=
XM_017009177.1:c.4190C=	XP_016864666.1:p.Pro1397=
XM_017009178.1:c.3095C=	XP_016864667.1:p.Pro1032=
XM_017009179.2:c.3095C=	XP_016864668.1:p.Pro1032=
XM_017009180.1:c.4190C=	XP_016864669.1:p.Pro1397=
XM_017009181.1:c.4190C=	XP_016864670.1:p.Pro1397=
XM_017009182.1:c.4190C=	XP_016864671.1:p.Pro1397=
XM_017009183.1:c.4190C=	XP_016864672.1:p.Pro1397=
XM_017009184.1:c.4190C=	XP_016864673.1:p.Pro1397=
XM_017009187.1:c.4190C=	XP_016864676.1:p.Pro1397=
XM_024454388.1:c.3095C=	XP_024310156.1:p.Pro1032=
XM_024454389.1:c.2684C=	XP_024310157.1:p.Pro895=
XR_001742034.1:n.4207C=
XR_001742035.1:n.4207C=
NM_001369.3:c.4082C= MANE Select	NP_001360.1:p.Pro1361=