Canonical Allele Identifier: CA1528465076

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13844993C= , CM000667.2:g.13844993C=	GRCh38
NC_000005.9:g.13845102C= , CM000667.1:g.13845102C=	GRCh37
NC_000005.8:g.13898102C=	NCBI36
NG_013081.1:g.104488G=
NG_013081.2:g.104488G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5115G= MANE Select	ENSP00000265104.4:p.Gly1705=
ENST00000681290.1:c.5070G=	ENSP00000505288.1:p.Gly1690=
ENST00000265104.4:c.5115G=	ENSP00000265104.4:p.Gly1705=
NM_001369.2:c.5115G=	NP_001360.1:p.Gly1705=
XM_005248262.2:c.5070G=	XP_005248319.1:p.Gly1690=
XM_011513990.1:c.5115G=	XP_011512292.1:p.Gly1705=
XR_925598.1:n.5322G=
XM_005248262.3:c.5223G=	XP_005248319.2:p.Gly1741=
XM_017009177.1:c.5223G=	XP_016864666.1:p.Gly1741=
XM_017009178.1:c.4128G=	XP_016864667.1:p.Gly1376=
XM_017009179.2:c.4128G=	XP_016864668.1:p.Gly1376=
XM_017009180.1:c.5223G=	XP_016864669.1:p.Gly1741=
XM_017009181.1:c.5223G=	XP_016864670.1:p.Gly1741=
XM_017009182.1:c.5223G=	XP_016864671.1:p.Gly1741=
XM_017009183.1:c.5223G=	XP_016864672.1:p.Gly1741=
XM_017009184.1:c.5223G=	XP_016864673.1:p.Gly1741=
XM_017009185.1:c.312G=	XP_016864674.1:p.Gly104=
XM_017009186.1:c.22-3089G=	XP_016864675.1:n.22-3089G=
XM_017009187.1:c.5223G=	XP_016864676.1:p.Gly1741=
XM_024454388.1:c.4128G=	XP_024310156.1:p.Gly1376=
XM_024454389.1:c.3717G=	XP_024310157.1:p.Gly1239=
XR_001742034.1:n.5240G=
XR_001742035.1:n.5240G=
NM_001369.3:c.5115G= MANE Select	NP_001360.1:p.Gly1705=