Canonical Allele Identifier: CA1528423549

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753527A= , CM000667.2:g.13753527A=	GRCh38
NC_000005.9:g.13753636A= , CM000667.1:g.13753636A=	GRCh37
NC_000005.8:g.13806636A=	NCBI36
NG_013081.1:g.195954T=
NG_013081.2:g.195954T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10578T= MANE Select	ENSP00000265104.4:p.Ala3526=
ENST00000681290.1:c.10533T=	ENSP00000505288.1:p.Ala3511=
ENST00000265104.4:c.10578T=	ENSP00000265104.4:p.Ala3526=
NM_001369.2:c.10578T=	NP_001360.1:p.Ala3526=
XM_005248262.2:c.10533T=	XP_005248319.1:p.Ala3511=
XM_005248262.3:c.10686T=	XP_005248319.2:p.Ala3562=
XM_017009177.1:c.10686T=	XP_016864666.1:p.Ala3562=
XM_017009178.1:c.9591T=	XP_016864667.1:p.Ala3197=
XM_017009179.2:c.9591T=	XP_016864668.1:p.Ala3197=
XM_017009180.1:c.10686T=	XP_016864669.1:p.Ala3562=
XM_017009181.1:c.10686T=	XP_016864670.1:p.Ala3562=
XM_017009182.1:c.10686T=	XP_016864671.1:p.Ala3562=
XM_017009185.1:c.5775T=	XP_016864674.1:p.Ala1925=
XM_017009186.1:c.5328T=	XP_016864675.1:p.Ala1776=
XM_017009188.1:c.4665T=	XP_016864677.1:p.Ala1555=
XM_024454388.1:c.9591T=	XP_024310156.1:p.Ala3197=
XM_024454389.1:c.9180T=	XP_024310157.1:p.Ala3060=
NM_001369.3:c.10578T= MANE Select	NP_001360.1:p.Ala3526=