Canonical Allele Identifier: CA359219269

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13792216T>A (hg19) ; chr5:g.13792107T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13792107T>A , CM000667.2:g.13792107T>A	GRCh38
NC_000005.9:g.13792216T>A , CM000667.1:g.13792216T>A	GRCh37
NC_000005.8:g.13845216T>A	NCBI36
NG_013081.1:g.157374A>T
NG_013081.2:g.157374A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8335A>T MANE Select	ENSP00000265104.4:p.Ile2779Phe
ENST00000681290.1:c.8290A>T	ENSP00000505288.1:p.Ile2764Phe
ENST00000265104.4:c.8335A>T	ENSP00000265104.4:p.Ile2779Phe
NM_001369.2:c.8335A>T	NP_001360.1:p.Ile2779Phe
XM_005248262.2:c.8290A>T	XP_005248319.1:p.Ile2764Phe
XM_011513990.1:c.8335A>T	XP_011512292.1:p.Ile2779Phe
XR_925598.1:n.8542A>T
XM_005248262.3:c.8443A>T	XP_005248319.2:p.Ile2815Phe
XM_017009177.1:c.8443A>T	XP_016864666.1:p.Ile2815Phe
XM_017009178.1:c.7348A>T	XP_016864667.1:p.Ile2450Phe
XM_017009179.2:c.7348A>T	XP_016864668.1:p.Ile2450Phe
XM_017009180.1:c.8443A>T	XP_016864669.1:p.Ile2815Phe
XM_017009181.1:c.8443A>T	XP_016864670.1:p.Ile2815Phe
XM_017009182.1:c.8443A>T	XP_016864671.1:p.Ile2815Phe
XM_017009183.1:c.8443A>T	XP_016864672.1:p.Ile2815Phe
XM_017009184.1:c.8443A>T	XP_016864673.1:p.Ile2815Phe
XM_017009185.1:c.3532A>T	XP_016864674.1:p.Ile1178Phe
XM_017009186.1:c.3085A>T	XP_016864675.1:p.Ile1029Phe
XM_017009188.1:c.2422A>T	XP_016864677.1:p.Ile808Phe
XM_024454388.1:c.7348A>T	XP_024310156.1:p.Ile2450Phe
XM_024454389.1:c.6937A>T	XP_024310157.1:p.Ile2313Phe
XR_001742034.1:n.8460A>T
XR_001742035.1:n.8460A>T
NM_001369.3:c.8335A>T MANE Select	NP_001360.1:p.Ile2779Phe