Canonical Allele Identifier: CA1528422929

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13752177T= , CM000667.2:g.13752177T=	GRCh38
NC_000005.9:g.13752286T= , CM000667.1:g.13752286T=	GRCh37
NC_000005.8:g.13805286T=	NCBI36
NG_013081.1:g.197304A=
NG_013081.2:g.197304A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10985A= MANE Select	ENSP00000265104.4:p.Asn3662=
ENST00000681290.1:c.10940A=	ENSP00000505288.1:p.Asn3647=
ENST00000265104.4:c.10985A=	ENSP00000265104.4:p.Asn3662=
NM_001369.2:c.10985A=	NP_001360.1:p.Asn3662=
XM_005248262.2:c.10940A=	XP_005248319.1:p.Asn3647=
XM_005248262.3:c.11093A=	XP_005248319.2:p.Asn3698=
XM_017009177.1:c.11093A=	XP_016864666.1:p.Asn3698=
XM_017009178.1:c.9998A=	XP_016864667.1:p.Asn3333=
XM_017009179.2:c.9998A=	XP_016864668.1:p.Asn3333=
XM_017009180.1:c.11093A=	XP_016864669.1:p.Asn3698=
XM_017009181.1:c.11093A=	XP_016864670.1:p.Asn3698=
XM_017009182.1:c.11093A=	XP_016864671.1:p.Asn3698=
XM_017009185.1:c.6182A=	XP_016864674.1:p.Asn2061=
XM_017009186.1:c.5735A=	XP_016864675.1:p.Asn1912=
XM_017009188.1:c.5072A=	XP_016864677.1:p.Asn1691=
XM_024454388.1:c.9998A=	XP_024310156.1:p.Asn3333=
XM_024454389.1:c.9587A=	XP_024310157.1:p.Asn3196=
NM_001369.3:c.10985A= MANE Select	NP_001360.1:p.Asn3662=