Canonical Allele Identifier: CA1528441640

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793562A= , CM000667.2:g.13793562A=	GRCh38
NC_000005.9:g.13793671A= , CM000667.1:g.13793671A=	GRCh37
NC_000005.8:g.13846671A=	NCBI36
NG_013081.1:g.155919T=
NG_013081.2:g.155919T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8177T= MANE Select	ENSP00000265104.4:p.Ile2726=
ENST00000681290.1:c.8132T=	ENSP00000505288.1:p.Ile2711=
ENST00000265104.4:c.8177T=	ENSP00000265104.4:p.Ile2726=
NM_001369.2:c.8177T=	NP_001360.1:p.Ile2726=
XM_005248262.2:c.8132T=	XP_005248319.1:p.Ile2711=
XM_011513990.1:c.8177T=	XP_011512292.1:p.Ile2726=
XR_925598.1:n.8384T=
XM_005248262.3:c.8285T=	XP_005248319.2:p.Ile2762=
XM_017009177.1:c.8285T=	XP_016864666.1:p.Ile2762=
XM_017009178.1:c.7190T=	XP_016864667.1:p.Ile2397=
XM_017009179.2:c.7190T=	XP_016864668.1:p.Ile2397=
XM_017009180.1:c.8285T=	XP_016864669.1:p.Ile2762=
XM_017009181.1:c.8285T=	XP_016864670.1:p.Ile2762=
XM_017009182.1:c.8285T=	XP_016864671.1:p.Ile2762=
XM_017009183.1:c.8285T=	XP_016864672.1:p.Ile2762=
XM_017009184.1:c.8285T=	XP_016864673.1:p.Ile2762=
XM_017009185.1:c.3374T=	XP_016864674.1:p.Ile1125=
XM_017009186.1:c.2927T=	XP_016864675.1:p.Ile976=
XM_017009188.1:c.2264T=	XP_016864677.1:p.Ile755=
XM_024454388.1:c.7190T=	XP_024310156.1:p.Ile2397=
XM_024454389.1:c.6779T=	XP_024310157.1:p.Ile2260=
XR_001742034.1:n.8302T=
XR_001742035.1:n.8302T=
NM_001369.3:c.8177T= MANE Select	NP_001360.1:p.Ile2726=