Canonical Allele Identifier: CA1528441622

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793520A= , CM000667.2:g.13793520A=	GRCh38
NC_000005.9:g.13793629A= , CM000667.1:g.13793629A=	GRCh37
NC_000005.8:g.13846629A=	NCBI36
NG_013081.1:g.155961T=
NG_013081.2:g.155961T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8219T= MANE Select	ENSP00000265104.4:p.Ile2740=
ENST00000681290.1:c.8174T=	ENSP00000505288.1:p.Ile2725=
ENST00000265104.4:c.8219T=	ENSP00000265104.4:p.Ile2740=
NM_001369.2:c.8219T=	NP_001360.1:p.Ile2740=
XM_005248262.2:c.8174T=	XP_005248319.1:p.Ile2725=
XM_011513990.1:c.8219T=	XP_011512292.1:p.Ile2740=
XR_925598.1:n.8426T=
XM_005248262.3:c.8327T=	XP_005248319.2:p.Ile2776=
XM_017009177.1:c.8327T=	XP_016864666.1:p.Ile2776=
XM_017009178.1:c.7232T=	XP_016864667.1:p.Ile2411=
XM_017009179.2:c.7232T=	XP_016864668.1:p.Ile2411=
XM_017009180.1:c.8327T=	XP_016864669.1:p.Ile2776=
XM_017009181.1:c.8327T=	XP_016864670.1:p.Ile2776=
XM_017009182.1:c.8327T=	XP_016864671.1:p.Ile2776=
XM_017009183.1:c.8327T=	XP_016864672.1:p.Ile2776=
XM_017009184.1:c.8327T=	XP_016864673.1:p.Ile2776=
XM_017009185.1:c.3416T=	XP_016864674.1:p.Ile1139=
XM_017009186.1:c.2969T=	XP_016864675.1:p.Ile990=
XM_017009188.1:c.2306T=	XP_016864677.1:p.Ile769=
XM_024454388.1:c.7232T=	XP_024310156.1:p.Ile2411=
XM_024454389.1:c.6821T=	XP_024310157.1:p.Ile2274=
XR_001742034.1:n.8344T=
XR_001742035.1:n.8344T=
NM_001369.3:c.8219T= MANE Select	NP_001360.1:p.Ile2740=