Canonical Allele Identifier: CA443266090

Gene: DNAH5

Linked Data

• ClinVar Variation Id: 1153443
• ClinVar RCV Id: RCV001495102
• dbSNP Id: rs2126910344
• MyVariant Identifiers: chr5:g.13793715A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793606A>C , CM000667.2:g.13793606A>C	GRCh38
NC_000005.9:g.13793715A>C , CM000667.1:g.13793715A>C	GRCh37
NC_000005.8:g.13846715A>C	NCBI36
NG_013081.1:g.155875T>G
NG_013081.2:g.155875T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8133T>G MANE Select	ENSP00000265104.4:p.Gly2711=
ENST00000681290.1:c.8088T>G	ENSP00000505288.1:p.Gly2696=
ENST00000265104.4:c.8133T>G	ENSP00000265104.4:p.Gly2711=
NM_001369.2:c.8133T>G	NP_001360.1:p.Gly2711=
XM_005248262.2:c.8088T>G	XP_005248319.1:p.Gly2696=
XM_011513990.1:c.8133T>G	XP_011512292.1:p.Gly2711=
XR_925598.1:n.8340T>G
XM_005248262.3:c.8241T>G	XP_005248319.2:p.Gly2747=
XM_017009177.1:c.8241T>G	XP_016864666.1:p.Gly2747=
XM_017009178.1:c.7146T>G	XP_016864667.1:p.Gly2382=
XM_017009179.2:c.7146T>G	XP_016864668.1:p.Gly2382=
XM_017009180.1:c.8241T>G	XP_016864669.1:p.Gly2747=
XM_017009181.1:c.8241T>G	XP_016864670.1:p.Gly2747=
XM_017009182.1:c.8241T>G	XP_016864671.1:p.Gly2747=
XM_017009183.1:c.8241T>G	XP_016864672.1:p.Gly2747=
XM_017009184.1:c.8241T>G	XP_016864673.1:p.Gly2747=
XM_017009185.1:c.3330T>G	XP_016864674.1:p.Gly1110=
XM_017009186.1:c.2883T>G	XP_016864675.1:p.Gly961=
XM_017009188.1:c.2220T>G	XP_016864677.1:p.Gly740=
XM_024454388.1:c.7146T>G	XP_024310156.1:p.Gly2382=
XM_024454389.1:c.6735T>G	XP_024310157.1:p.Gly2245=
XR_001742034.1:n.8258T>G
XR_001742035.1:n.8258T>G
NM_001369.3:c.8133T>G MANE Select	NP_001360.1:p.Gly2711=