Canonical Allele Identifier: CA359221748

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13794045C>A (hg19) ; chr5:g.13793936C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793936C>A , CM000667.2:g.13793936C>A	GRCh38
NC_000005.9:g.13794045C>A , CM000667.1:g.13794045C>A	GRCh37
NC_000005.8:g.13847045C>A	NCBI36
NG_013081.1:g.155545G>T
NG_013081.2:g.155545G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.8010G>T MANE Select	ENSP00000265104.4:p.Gln2670His
ENST00000681290.1:c.7965G>T	ENSP00000505288.1:p.Gln2655His
ENST00000265104.4:c.8010G>T	ENSP00000265104.4:p.Gln2670His
NM_001369.2:c.8010G>T	NP_001360.1:p.Gln2670His
XM_005248262.2:c.7965G>T	XP_005248319.1:p.Gln2655His
XM_011513990.1:c.8010G>T	XP_011512292.1:p.Gln2670His
XR_925598.1:n.8217G>T
XM_005248262.3:c.8118G>T	XP_005248319.2:p.Gln2706His
XM_017009177.1:c.8118G>T	XP_016864666.1:p.Gln2706His
XM_017009178.1:c.7023G>T	XP_016864667.1:p.Gln2341His
XM_017009179.2:c.7023G>T	XP_016864668.1:p.Gln2341His
XM_017009180.1:c.8118G>T	XP_016864669.1:p.Gln2706His
XM_017009181.1:c.8118G>T	XP_016864670.1:p.Gln2706His
XM_017009182.1:c.8118G>T	XP_016864671.1:p.Gln2706His
XM_017009183.1:c.8118G>T	XP_016864672.1:p.Gln2706His
XM_017009184.1:c.8118G>T	XP_016864673.1:p.Gln2706His
XM_017009185.1:c.3207G>T	XP_016864674.1:p.Gln1069His
XM_017009186.1:c.2760G>T	XP_016864675.1:p.Gln920His
XM_017009188.1:c.2097G>T	XP_016864677.1:p.Gln699His
XM_024454388.1:c.7023G>T	XP_024310156.1:p.Gln2341His
XM_024454389.1:c.6612G>T	XP_024310157.1:p.Gln2204His
XR_001742034.1:n.8135G>T
XR_001742035.1:n.8135G>T
NM_001369.3:c.8010G>T MANE Select	NP_001360.1:p.Gln2670His