Canonical Allele Identifier: CA359211863

Gene: DNAH5

Linked Data

• dbSNP Id: rs1303701419
• gnomAD v4: 5-13841834-G-A
• MyVariant Identifiers: chr5:g.13841943G>A (hg19) ; chr5:g.13841834G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13841834G>A , CM000667.2:g.13841834G>A	GRCh38
NC_000005.9:g.13841943G>A , CM000667.1:g.13841943G>A	GRCh37
NC_000005.8:g.13894943G>A	NCBI36
NG_013081.1:g.107647C>T
NG_013081.2:g.107647C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5342C>T MANE Select	ENSP00000265104.4:p.Ala1781Val
ENST00000681290.1:c.5297C>T	ENSP00000505288.1:p.Ala1766Val
ENST00000265104.4:c.5342C>T	ENSP00000265104.4:p.Ala1781Val
NM_001369.2:c.5342C>T	NP_001360.1:p.Ala1781Val
XM_005248262.2:c.5297C>T	XP_005248319.1:p.Ala1766Val
XM_011513990.1:c.5342C>T	XP_011512292.1:p.Ala1781Val
XR_925598.1:n.5549C>T
XM_005248262.3:c.5450C>T	XP_005248319.2:p.Ala1817Val
XM_017009177.1:c.5450C>T	XP_016864666.1:p.Ala1817Val
XM_017009178.1:c.4355C>T	XP_016864667.1:p.Ala1452Val
XM_017009179.2:c.4355C>T	XP_016864668.1:p.Ala1452Val
XM_017009180.1:c.5450C>T	XP_016864669.1:p.Ala1817Val
XM_017009181.1:c.5450C>T	XP_016864670.1:p.Ala1817Val
XM_017009182.1:c.5450C>T	XP_016864671.1:p.Ala1817Val
XM_017009183.1:c.5450C>T	XP_016864672.1:p.Ala1817Val
XM_017009184.1:c.5450C>T	XP_016864673.1:p.Ala1817Val
XM_017009185.1:c.539C>T	XP_016864674.1:p.Ala180Val
XM_017009186.1:c.92C>T	XP_016864675.1:p.Ala31Val
XM_017009187.1:c.5450C>T	XP_016864676.1:p.Ala1817Val
XM_024454388.1:c.4355C>T	XP_024310156.1:p.Ala1452Val
XM_024454389.1:c.3944C>T	XP_024310157.1:p.Ala1315Val
XR_001742034.1:n.5467C>T
XR_001742035.1:n.5467C>T
NM_001369.3:c.5342C>T MANE Select	NP_001360.1:p.Ala1781Val