Canonical Allele Identifier: CA359199326

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13829517-G-A
• MyVariant Identifiers: chr5:g.13829626G>A (hg19) ; chr5:g.13829517G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13829517G>A , CM000667.2:g.13829517G>A	GRCh38
NC_000005.9:g.13829626G>A , CM000667.1:g.13829626G>A	GRCh37
NC_000005.8:g.13882626G>A	NCBI36
NG_013081.1:g.119964C>T
NG_013081.2:g.119964C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000683090.1:n.1368C>T
ENST00000265104.5:c.6437C>T MANE Select	ENSP00000265104.4:p.Ser2146Phe
ENST00000681290.1:c.6392C>T	ENSP00000505288.1:p.Ser2131Phe
ENST00000265104.4:c.6437C>T	ENSP00000265104.4:p.Ser2146Phe
NM_001369.2:c.6437C>T	NP_001360.1:p.Ser2146Phe
XM_005248262.2:c.6392C>T	XP_005248319.1:p.Ser2131Phe
XM_011513990.1:c.6437C>T	XP_011512292.1:p.Ser2146Phe
XR_925598.1:n.6644C>T
XM_005248262.3:c.6545C>T	XP_005248319.2:p.Ser2182Phe
XM_017009177.1:c.6545C>T	XP_016864666.1:p.Ser2182Phe
XM_017009178.1:c.5450C>T	XP_016864667.1:p.Ser1817Phe
XM_017009179.2:c.5450C>T	XP_016864668.1:p.Ser1817Phe
XM_017009180.1:c.6545C>T	XP_016864669.1:p.Ser2182Phe
XM_017009181.1:c.6545C>T	XP_016864670.1:p.Ser2182Phe
XM_017009182.1:c.6545C>T	XP_016864671.1:p.Ser2182Phe
XM_017009183.1:c.6545C>T	XP_016864672.1:p.Ser2182Phe
XM_017009184.1:c.6545C>T	XP_016864673.1:p.Ser2182Phe
XM_017009185.1:c.1634C>T	XP_016864674.1:p.Ser545Phe
XM_017009186.1:c.1187C>T	XP_016864675.1:p.Ser396Phe
XM_017009187.1:c.6545C>T	XP_016864676.1:p.Ser2182Phe
XM_017009188.1:c.524C>T	XP_016864677.1:p.Ser175Phe
XM_024454388.1:c.5450C>T	XP_024310156.1:p.Ser1817Phe
XM_024454389.1:c.5039C>T	XP_024310157.1:p.Ser1680Phe
XR_001742034.1:n.6562C>T
XR_001742035.1:n.6562C>T
NM_001369.3:c.6437C>T MANE Select	NP_001360.1:p.Ser2146Phe