Canonical Allele Identifier: CA3202637

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13777273T>A , CM000667.2:g.13777273T>A	GRCh38
NC_000005.9:g.13777382T>A , CM000667.1:g.13777382T>A	GRCh37
NC_000005.8:g.13830382T>A	NCBI36
NG_013081.1:g.172208A>T
NG_013081.2:g.172208A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.9034A>T MANE Select	NP_001360.1:p.Ile3012Phe
ENST00000265104.5:c.9034A>T MANE Select	ENSP00000265104.4:p.Ile3012Phe
NM_001369.2:c.9034A>T	NP_001360.1:p.Ile3012Phe
ENST00000265104.4:c.9034A>T	ENSP00000265104.4:p.Ile3012Phe
ENST00000681290.1:c.8989A>T	ENSP00000505288.1:p.Ile2997Phe
XM_005248262.2:c.8989A>T	XP_005248319.1:p.Ile2997Phe
XM_005248262.3:c.9142A>T	XP_005248319.2:p.Ile3048Phe
XM_011513990.1:c.9034A>T	XP_011512292.1:p.Ile3012Phe
XM_017009177.1:c.9142A>T	XP_016864666.1:p.Ile3048Phe
XM_017009178.1:c.8047A>T	XP_016864667.1:p.Ile2683Phe
XM_017009179.2:c.8047A>T	XP_016864668.1:p.Ile2683Phe
XM_017009180.1:c.9142A>T	XP_016864669.1:p.Ile3048Phe
XM_017009181.1:c.9142A>T	XP_016864670.1:p.Ile3048Phe
XM_017009182.1:c.9142A>T	XP_016864671.1:p.Ile3048Phe
XM_017009183.1:c.9142A>T	XP_016864672.1:p.Ile3048Phe
XM_017009184.1:c.9142A>T	XP_016864673.1:p.Ile3048Phe
XM_017009185.1:c.4231A>T	XP_016864674.1:p.Ile1411Phe
XM_017009186.1:c.3784A>T	XP_016864675.1:p.Ile1262Phe
XM_017009188.1:c.3121A>T	XP_016864677.1:p.Ile1041Phe
XM_024454388.1:c.8047A>T	XP_024310156.1:p.Ile2683Phe
XM_024454389.1:c.7636A>T	XP_024310157.1:p.Ile2546Phe
XR_001742034.1:n.9028A>T
XR_001742035.1:n.9028A>T
XR_925598.1:n.9110A>T