Canonical Allele Identifier: CA443263393

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13792145C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13792036C>T , CM000667.2:g.13792036C>T	GRCh38
NC_000005.9:g.13792145C>T , CM000667.1:g.13792145C>T	GRCh37
NC_000005.8:g.13845145C>T	NCBI36
NG_013081.1:g.157445G>A
NG_013081.2:g.157445G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.8406G>A MANE Select	ENSP00000265104.4:p.Gln2802=
ENST00000681290.1:c.8361G>A	ENSP00000505288.1:p.Gln2787=
ENST00000265104.4:c.8406G>A	ENSP00000265104.4:p.Gln2802=
NM_001369.2:c.8406G>A	NP_001360.1:p.Gln2802=
XM_005248262.2:c.8361G>A	XP_005248319.1:p.Gln2787=
XM_011513990.1:c.8406G>A	XP_011512292.1:p.Gln2802=
XR_925598.1:n.8613G>A
XM_005248262.3:c.8514G>A	XP_005248319.2:p.Gln2838=
XM_017009177.1:c.8514G>A	XP_016864666.1:p.Gln2838=
XM_017009178.1:c.7419G>A	XP_016864667.1:p.Gln2473=
XM_017009179.2:c.7419G>A	XP_016864668.1:p.Gln2473=
XM_017009180.1:c.8514G>A	XP_016864669.1:p.Gln2838=
XM_017009181.1:c.8514G>A	XP_016864670.1:p.Gln2838=
XM_017009182.1:c.8514G>A	XP_016864671.1:p.Gln2838=
XM_017009183.1:c.8514G>A	XP_016864672.1:p.Gln2838=
XM_017009184.1:c.8514G>A	XP_016864673.1:p.Gln2838=
XM_017009185.1:c.3603G>A	XP_016864674.1:p.Gln1201=
XM_017009186.1:c.3156G>A	XP_016864675.1:p.Gln1052=
XM_017009188.1:c.2493G>A	XP_016864677.1:p.Gln831=
XM_024454388.1:c.7419G>A	XP_024310156.1:p.Gln2473=
XM_024454389.1:c.7008G>A	XP_024310157.1:p.Gln2336=
XR_001742034.1:n.8531G>A
XR_001742035.1:n.8531G>A
NM_001369.3:c.8406G>A MANE Select	NP_001360.1:p.Gln2802=