Canonical Allele Identifier: CA359221572

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13793806T>G (hg19) ; chr5:g.13793697T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793697T>G , CM000667.2:g.13793697T>G	GRCh38
NC_000005.9:g.13793806T>G , CM000667.1:g.13793806T>G	GRCh37
NC_000005.8:g.13846806T>G	NCBI36
NG_013081.1:g.155784A>C
NG_013081.2:g.155784A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8042A>C MANE Select	ENSP00000265104.4:p.Glu2681Ala
ENST00000681290.1:c.7997A>C	ENSP00000505288.1:p.Glu2666Ala
ENST00000265104.4:c.8042A>C	ENSP00000265104.4:p.Glu2681Ala
NM_001369.2:c.8042A>C	NP_001360.1:p.Glu2681Ala
XM_005248262.2:c.7997A>C	XP_005248319.1:p.Glu2666Ala
XM_011513990.1:c.8042A>C	XP_011512292.1:p.Glu2681Ala
XR_925598.1:n.8249A>C
XM_005248262.3:c.8150A>C	XP_005248319.2:p.Glu2717Ala
XM_017009177.1:c.8150A>C	XP_016864666.1:p.Glu2717Ala
XM_017009178.1:c.7055A>C	XP_016864667.1:p.Glu2352Ala
XM_017009179.2:c.7055A>C	XP_016864668.1:p.Glu2352Ala
XM_017009180.1:c.8150A>C	XP_016864669.1:p.Glu2717Ala
XM_017009181.1:c.8150A>C	XP_016864670.1:p.Glu2717Ala
XM_017009182.1:c.8150A>C	XP_016864671.1:p.Glu2717Ala
XM_017009183.1:c.8150A>C	XP_016864672.1:p.Glu2717Ala
XM_017009184.1:c.8150A>C	XP_016864673.1:p.Glu2717Ala
XM_017009185.1:c.3239A>C	XP_016864674.1:p.Glu1080Ala
XM_017009186.1:c.2792A>C	XP_016864675.1:p.Glu931Ala
XM_017009188.1:c.2129A>C	XP_016864677.1:p.Glu710Ala
XM_024454388.1:c.7055A>C	XP_024310156.1:p.Glu2352Ala
XM_024454389.1:c.6644A>C	XP_024310157.1:p.Glu2215Ala
XR_001742034.1:n.8167A>C
XR_001742035.1:n.8167A>C
NM_001369.3:c.8042A>C MANE Select	NP_001360.1:p.Glu2681Ala