Canonical Allele Identifier: CA359221211

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13793689A>C (hg19) ; chr5:g.13793580A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793580A>C , CM000667.2:g.13793580A>C	GRCh38
NC_000005.9:g.13793689A>C , CM000667.1:g.13793689A>C	GRCh37
NC_000005.8:g.13846689A>C	NCBI36
NG_013081.1:g.155901T>G
NG_013081.2:g.155901T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8159T>G MANE Select	ENSP00000265104.4:p.Leu2720Arg
ENST00000681290.1:c.8114T>G	ENSP00000505288.1:p.Leu2705Arg
ENST00000265104.4:c.8159T>G	ENSP00000265104.4:p.Leu2720Arg
NM_001369.2:c.8159T>G	NP_001360.1:p.Leu2720Arg
XM_005248262.2:c.8114T>G	XP_005248319.1:p.Leu2705Arg
XM_011513990.1:c.8159T>G	XP_011512292.1:p.Leu2720Arg
XR_925598.1:n.8366T>G
XM_005248262.3:c.8267T>G	XP_005248319.2:p.Leu2756Arg
XM_017009177.1:c.8267T>G	XP_016864666.1:p.Leu2756Arg
XM_017009178.1:c.7172T>G	XP_016864667.1:p.Leu2391Arg
XM_017009179.2:c.7172T>G	XP_016864668.1:p.Leu2391Arg
XM_017009180.1:c.8267T>G	XP_016864669.1:p.Leu2756Arg
XM_017009181.1:c.8267T>G	XP_016864670.1:p.Leu2756Arg
XM_017009182.1:c.8267T>G	XP_016864671.1:p.Leu2756Arg
XM_017009183.1:c.8267T>G	XP_016864672.1:p.Leu2756Arg
XM_017009184.1:c.8267T>G	XP_016864673.1:p.Leu2756Arg
XM_017009185.1:c.3356T>G	XP_016864674.1:p.Leu1119Arg
XM_017009186.1:c.2909T>G	XP_016864675.1:p.Leu970Arg
XM_017009188.1:c.2246T>G	XP_016864677.1:p.Leu749Arg
XM_024454388.1:c.7172T>G	XP_024310156.1:p.Leu2391Arg
XM_024454389.1:c.6761T>G	XP_024310157.1:p.Leu2254Arg
XR_001742034.1:n.8284T>G
XR_001742035.1:n.8284T>G
NM_001369.3:c.8159T>G MANE Select	NP_001360.1:p.Leu2720Arg