Canonical Allele Identifier: CA359201241

Gene: DNAH5

Linked Data

• ClinVar Variation Id: 2170297
• ClinVar RCV Id: RCV003085268
• gnomAD v4: 5-13768967-G-A
• MyVariant Identifiers: chr5:g.13769076G>A (hg19) ; chr5:g.13768967G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13768967G>A , CM000667.2:g.13768967G>A	GRCh38
NC_000005.9:g.13769076G>A , CM000667.1:g.13769076G>A	GRCh37
NC_000005.8:g.13822076G>A	NCBI36
NG_013081.1:g.180514C>T
NG_013081.2:g.180514C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9890C>T MANE Select	ENSP00000265104.4:p.Ala3297Val
ENST00000681290.1:c.9845C>T	ENSP00000505288.1:p.Ala3282Val
ENST00000265104.4:c.9890C>T	ENSP00000265104.4:p.Ala3297Val
ENST00000504001.3:n.602C>T
NM_001369.2:c.9890C>T	NP_001360.1:p.Ala3297Val
XM_005248262.2:c.9845C>T	XP_005248319.1:p.Ala3282Val
XM_005248262.3:c.9998C>T	XP_005248319.2:p.Ala3333Val
XM_017009177.1:c.9998C>T	XP_016864666.1:p.Ala3333Val
XM_017009178.1:c.8903C>T	XP_016864667.1:p.Ala2968Val
XM_017009179.2:c.8903C>T	XP_016864668.1:p.Ala2968Val
XM_017009180.1:c.9998C>T	XP_016864669.1:p.Ala3333Val
XM_017009181.1:c.9998C>T	XP_016864670.1:p.Ala3333Val
XM_017009182.1:c.9998C>T	XP_016864671.1:p.Ala3333Val
XM_017009185.1:c.5087C>T	XP_016864674.1:p.Ala1696Val
XM_017009186.1:c.4640C>T	XP_016864675.1:p.Ala1547Val
XM_017009188.1:c.3977C>T	XP_016864677.1:p.Ala1326Val
XM_024454388.1:c.8903C>T	XP_024310156.1:p.Ala2968Val
XM_024454389.1:c.8492C>T	XP_024310157.1:p.Ala2831Val
NM_001369.3:c.9890C>T MANE Select	NP_001360.1:p.Ala3297Val