Canonical Allele Identifier: CA359209794

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13776800C>T (hg19) ; chr5:g.13776691C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776691C>T , CM000667.2:g.13776691C>T	GRCh38
NC_000005.9:g.13776800C>T , CM000667.1:g.13776800C>T	GRCh37
NC_000005.8:g.13829800C>T	NCBI36
NG_013081.1:g.172790G>A
NG_013081.2:g.172790G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9121G>A MANE Select	ENSP00000265104.4:p.Ala3041Thr
ENST00000681290.1:c.9076G>A	ENSP00000505288.1:p.Ala3026Thr
ENST00000265104.4:c.9121G>A	ENSP00000265104.4:p.Ala3041Thr
NM_001369.2:c.9121G>A	NP_001360.1:p.Ala3041Thr
XM_005248262.2:c.9076G>A	XP_005248319.1:p.Ala3026Thr
XM_011513990.1:c.*8G>A	XP_011512292.1:n.*8G>A
XR_925598.1:n.9192G>A
XM_005248262.3:c.9229G>A	XP_005248319.2:p.Ala3077Thr
XM_017009177.1:c.9229G>A	XP_016864666.1:p.Ala3077Thr
XM_017009178.1:c.8134G>A	XP_016864667.1:p.Ala2712Thr
XM_017009179.2:c.8134G>A	XP_016864668.1:p.Ala2712Thr
XM_017009180.1:c.9229G>A	XP_016864669.1:p.Ala3077Thr
XM_017009181.1:c.9229G>A	XP_016864670.1:p.Ala3077Thr
XM_017009182.1:c.9229G>A	XP_016864671.1:p.Ala3077Thr
XM_017009183.1:c.9229G>A	XP_016864672.1:p.Ala3077Thr
XM_017009184.1:c.*8G>A	XP_016864673.1:n.*8G>A
XM_017009185.1:c.4318G>A	XP_016864674.1:p.Ala1440Thr
XM_017009186.1:c.3871G>A	XP_016864675.1:p.Ala1291Thr
XM_017009188.1:c.3208G>A	XP_016864677.1:p.Ala1070Thr
XM_024454388.1:c.8134G>A	XP_024310156.1:p.Ala2712Thr
XM_024454389.1:c.7723G>A	XP_024310157.1:p.Ala2575Thr
XR_001742034.1:n.9115G>A
XR_001742035.1:n.9110G>A
NM_001369.3:c.9121G>A MANE Select	NP_001360.1:p.Ala3041Thr