Canonical Allele Identifier: CA359223211

Gene: DNAH5

Linked Data

• ClinVar Variation Id: 1725836
• ClinVar RCV Id: RCV002309520
• gnomAD v4: 5-13735224-C-A
• MyVariant Identifiers: chr5:g.13735333C>A (hg19) ; chr5:g.13735224C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13735224C>A , CM000667.2:g.13735224C>A	GRCh38
NC_000005.9:g.13735333C>A , CM000667.1:g.13735333C>A	GRCh37
NC_000005.8:g.13788333C>A	NCBI36
NG_013081.1:g.214257G>T
NG_013081.2:g.214257G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.11668G>T MANE Select	ENSP00000265104.4:p.Glu3890Ter
ENST00000681290.1:c.11623G>T	ENSP00000505288.1:p.Glu3875Ter
ENST00000265104.4:c.11668G>T	ENSP00000265104.4:p.Glu3890Ter
NM_001369.2:c.11668G>T	NP_001360.1:p.Glu3890Ter
XM_005248262.2:c.11623G>T	XP_005248319.1:p.Glu3875Ter
XM_005248262.3:c.11776G>T	XP_005248319.2:p.Glu3926Ter
XM_017009177.1:c.11776G>T	XP_016864666.1:p.Glu3926Ter
XM_017009178.1:c.10681G>T	XP_016864667.1:p.Glu3561Ter
XM_017009179.2:c.10681G>T	XP_016864668.1:p.Glu3561Ter
XM_017009180.1:c.11776G>T	XP_016864669.1:p.Glu3926Ter
XM_017009181.1:c.11776G>T	XP_016864670.1:p.Glu3926Ter
XM_017009185.1:c.6865G>T	XP_016864674.1:p.Glu2289Ter
XM_017009186.1:c.6418G>T	XP_016864675.1:p.Glu2140Ter
XM_017009188.1:c.5755G>T	XP_016864677.1:p.Glu1919Ter
XM_024454388.1:c.10681G>T	XP_024310156.1:p.Glu3561Ter
XM_024454389.1:c.10270G>T	XP_024310157.1:p.Glu3424Ter
NM_001369.3:c.11668G>T MANE Select	NP_001360.1:p.Glu3890Ter