Canonical Allele Identifier: CA359212704

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13780978A>T (hg19) ; chr5:g.13780869A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13780869A>T , CM000667.2:g.13780869A>T	GRCh38
NC_000005.9:g.13780978A>T , CM000667.1:g.13780978A>T	GRCh37
NC_000005.8:g.13833978A>T	NCBI36
NG_013081.1:g.168612T>A
NG_013081.2:g.168612T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.8911T>A MANE Select	ENSP00000265104.4:p.Phe2971Ile
ENST00000681290.1:c.8866T>A	ENSP00000505288.1:p.Phe2956Ile
ENST00000265104.4:c.8911T>A	ENSP00000265104.4:p.Phe2971Ile
NM_001369.2:c.8911T>A	NP_001360.1:p.Phe2971Ile
XM_005248262.2:c.8866T>A	XP_005248319.1:p.Phe2956Ile
XM_011513990.1:c.8911T>A	XP_011512292.1:p.Phe2971Ile
XR_925598.1:n.9028-3514T>A
XM_005248262.3:c.9019T>A	XP_005248319.2:p.Phe3007Ile
XM_017009177.1:c.9019T>A	XP_016864666.1:p.Phe3007Ile
XM_017009178.1:c.7924T>A	XP_016864667.1:p.Phe2642Ile
XM_017009179.2:c.7924T>A	XP_016864668.1:p.Phe2642Ile
XM_017009180.1:c.9019T>A	XP_016864669.1:p.Phe3007Ile
XM_017009181.1:c.9019T>A	XP_016864670.1:p.Phe3007Ile
XM_017009182.1:c.9019T>A	XP_016864671.1:p.Phe3007Ile
XM_017009183.1:c.9019T>A	XP_016864672.1:p.Phe3007Ile
XM_017009184.1:c.9019T>A	XP_016864673.1:p.Phe3007Ile
XM_017009185.1:c.4108T>A	XP_016864674.1:p.Phe1370Ile
XM_017009186.1:c.3661T>A	XP_016864675.1:p.Phe1221Ile
XM_017009188.1:c.2998T>A	XP_016864677.1:p.Phe1000Ile
XM_024454388.1:c.7924T>A	XP_024310156.1:p.Phe2642Ile
XM_024454389.1:c.7513T>A	XP_024310157.1:p.Phe2505Ile
XR_001742034.1:n.8946-3514T>A
XR_001742035.1:n.8946-3514T>A
NM_001369.3:c.8911T>A MANE Select	NP_001360.1:p.Phe2971Ile