Canonical Allele Identifier: CA359201833
Gene: DNAH5 HGNC NCBI

Linked Data

dbSNP Id: rs1752916666
gnomAD v3: 5-13769036-G-A
gnomAD v4: 5-13769036-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13769036G>A , CM000667.2:g.13769036G>A GRCh38
NC_000005.9:g.13769145G>A , CM000667.1:g.13769145G>A GRCh37
NC_000005.8:g.13822145G>A NCBI36
NG_013081.1:g.180445C>T
NG_013081.2:g.180445C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.9821C>T MANE Select ENSP00000265104.4:p.Ser3274Phe
ENST00000681290.1:c.9776C>T ENSP00000505288.1:p.Ser3259Phe
ENST00000265104.4:c.9821C>T ENSP00000265104.4:p.Ser3274Phe
ENST00000504001.3:n.533C>T
NM_001369.2:c.9821C>T NP_001360.1:p.Ser3274Phe
XM_005248262.2:c.9776C>T XP_005248319.1:p.Ser3259Phe
XM_005248262.3:c.9929C>T XP_005248319.2:p.Ser3310Phe
XM_017009177.1:c.9929C>T XP_016864666.1:p.Ser3310Phe
XM_017009178.1:c.8834C>T XP_016864667.1:p.Ser2945Phe
XM_017009179.2:c.8834C>T XP_016864668.1:p.Ser2945Phe
XM_017009180.1:c.9929C>T XP_016864669.1:p.Ser3310Phe
XM_017009181.1:c.9929C>T XP_016864670.1:p.Ser3310Phe
XM_017009182.1:c.9929C>T XP_016864671.1:p.Ser3310Phe
XM_017009185.1:c.5018C>T XP_016864674.1:p.Ser1673Phe
XM_017009186.1:c.4571C>T XP_016864675.1:p.Ser1524Phe
XM_017009188.1:c.3908C>T XP_016864677.1:p.Ser1303Phe
XM_024454388.1:c.8834C>T XP_024310156.1:p.Ser2945Phe
XM_024454389.1:c.8423C>T XP_024310157.1:p.Ser2808Phe
NM_001369.3:c.9821C>T MANE Select NP_001360.1:p.Ser3274Phe