Canonical Allele Identifier: CA1528435097

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776500G= , CM000667.2:g.13776500G=	GRCh38
NC_000005.9:g.13776609G= , CM000667.1:g.13776609G=	GRCh37
NC_000005.8:g.13829609G=	NCBI36
NG_013081.1:g.172981C=
NG_013081.2:g.172981C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9312C= MANE Select	ENSP00000265104.4:p.Ala3104=
ENST00000681290.1:c.9267C=	ENSP00000505288.1:p.Ala3089=
ENST00000265104.4:c.9312C=	ENSP00000265104.4:p.Ala3104=
NM_001369.2:c.9312C=	NP_001360.1:p.Ala3104=
XM_005248262.2:c.9267C=	XP_005248319.1:p.Ala3089=
XM_005248262.3:c.9420C=	XP_005248319.2:p.Ala3140=
XM_017009177.1:c.9420C=	XP_016864666.1:p.Ala3140=
XM_017009178.1:c.8325C=	XP_016864667.1:p.Ala2775=
XM_017009179.2:c.8325C=	XP_016864668.1:p.Ala2775=
XM_017009180.1:c.9420C=	XP_016864669.1:p.Ala3140=
XM_017009181.1:c.9420C=	XP_016864670.1:p.Ala3140=
XM_017009182.1:c.9420C=	XP_016864671.1:p.Ala3140=
XM_017009183.1:c.9420C=	XP_016864672.1:p.Ala3140=
XM_017009185.1:c.4509C=	XP_016864674.1:p.Ala1503=
XM_017009186.1:c.4062C=	XP_016864675.1:p.Ala1354=
XM_017009188.1:c.3399C=	XP_016864677.1:p.Ala1133=
XM_024454388.1:c.8325C=	XP_024310156.1:p.Ala2775=
XM_024454389.1:c.7914C=	XP_024310157.1:p.Ala2638=
NM_001369.3:c.9312C= MANE Select	NP_001360.1:p.Ala3104=