Canonical Allele Identifier: CA359199612

Gene: DNAH5

Linked Data

• ClinVar Variation Id: 454758
• ClinVar RCV Id: RCV000559049 ; RCV003403249
• dbSNP Id: rs1554092890
• MyVariant Identifiers: chr5:g.13891158A>T (hg19) ; chr5:g.13891049A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13891049A>T , CM000667.2:g.13891049A>T	GRCh38
NC_000005.9:g.13891158A>T , CM000667.1:g.13891158A>T	GRCh37
NC_000005.8:g.13944158A>T	NCBI36
NG_013081.1:g.58432T>A
NG_013081.2:g.58432T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.2504T>A MANE Select	ENSP00000265104.4:p.Met835Lys
ENST00000681290.1:c.2459T>A	ENSP00000505288.1:p.Met820Lys
ENST00000265104.4:c.2504T>A	ENSP00000265104.4:p.Met835Lys
NM_001369.2:c.2504T>A	NP_001360.1:p.Met835Lys
XM_005248262.2:c.2459T>A	XP_005248319.1:p.Met820Lys
XM_011513990.1:c.2504T>A	XP_011512292.1:p.Met835Lys
XR_925598.1:n.2711T>A
XM_005248262.3:c.2612T>A	XP_005248319.2:p.Met871Lys
XM_017009177.1:c.2612T>A	XP_016864666.1:p.Met871Lys
XM_017009178.1:c.1517T>A	XP_016864667.1:p.Met506Lys
XM_017009179.2:c.1517T>A	XP_016864668.1:p.Met506Lys
XM_017009180.1:c.2612T>A	XP_016864669.1:p.Met871Lys
XM_017009181.1:c.2612T>A	XP_016864670.1:p.Met871Lys
XM_017009182.1:c.2612T>A	XP_016864671.1:p.Met871Lys
XM_017009183.1:c.2612T>A	XP_016864672.1:p.Met871Lys
XM_017009184.1:c.2612T>A	XP_016864673.1:p.Met871Lys
XM_017009187.1:c.2612T>A	XP_016864676.1:p.Met871Lys
XM_024454388.1:c.1517T>A	XP_024310156.1:p.Met506Lys
XM_024454389.1:c.1106T>A	XP_024310157.1:p.Met369Lys
XR_001742034.1:n.2629T>A
XR_001742035.1:n.2629T>A
NM_001369.3:c.2504T>A MANE Select	NP_001360.1:p.Met835Lys