Canonical Allele Identifier: CA1528423511

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753438G= , CM000667.2:g.13753438G=	GRCh38
NC_000005.9:g.13753547G= , CM000667.1:g.13753547G=	GRCh37
NC_000005.8:g.13806547G=	NCBI36
NG_013081.1:g.196043C=
NG_013081.2:g.196043C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10667C= MANE Select	ENSP00000265104.4:p.Pro3556=
ENST00000681290.1:c.10622C=	ENSP00000505288.1:p.Pro3541=
ENST00000265104.4:c.10667C=	ENSP00000265104.4:p.Pro3556=
NM_001369.2:c.10667C=	NP_001360.1:p.Pro3556=
XM_005248262.2:c.10622C=	XP_005248319.1:p.Pro3541=
XM_005248262.3:c.10775C=	XP_005248319.2:p.Pro3592=
XM_017009177.1:c.10775C=	XP_016864666.1:p.Pro3592=
XM_017009178.1:c.9680C=	XP_016864667.1:p.Pro3227=
XM_017009179.2:c.9680C=	XP_016864668.1:p.Pro3227=
XM_017009180.1:c.10775C=	XP_016864669.1:p.Pro3592=
XM_017009181.1:c.10775C=	XP_016864670.1:p.Pro3592=
XM_017009182.1:c.10775C=	XP_016864671.1:p.Pro3592=
XM_017009185.1:c.5864C=	XP_016864674.1:p.Pro1955=
XM_017009186.1:c.5417C=	XP_016864675.1:p.Pro1806=
XM_017009188.1:c.4754C=	XP_016864677.1:p.Pro1585=
XM_024454388.1:c.9680C=	XP_024310156.1:p.Pro3227=
XM_024454389.1:c.9269C=	XP_024310157.1:p.Pro3090=
NM_001369.3:c.10667C= MANE Select	NP_001360.1:p.Pro3556=