Canonical Allele Identifier: CA1528395834

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13691986A= , CM000667.2:g.13691986A=	GRCh38
NC_000005.9:g.13692095A= , CM000667.1:g.13692095A=	GRCh37
NC_000005.8:g.13745095A=	NCBI36
NG_013081.1:g.257495T=
NG_013081.2:g.257495T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1206T=
ENST00000265104.5:c.13873T= MANE Select	ENSP00000265104.4:p.Ter4625=
ENST00000681290.1:c.13828T=	ENSP00000505288.1:p.Ter4610=
ENST00000265104.4:c.13873T=	ENSP00000265104.4:p.Ter4625=
NM_001369.2:c.13873T=	NP_001360.1:p.Ter4625=
XM_005248262.2:c.13828T=	XP_005248319.1:p.Ter4610=
XM_005248262.3:c.13981T=	XP_005248319.2:p.Ter4661=
XM_017009177.1:c.13561T=	XP_016864666.1:p.Ter4521=
XM_017009178.1:c.12886T=	XP_016864667.1:p.Ter4296=
XM_017009179.2:c.12886T=	XP_016864668.1:p.Ter4296=
XM_017009185.1:c.9070T=	XP_016864674.1:p.Ter3024=
XM_017009186.1:c.8623T=	XP_016864675.1:p.Ter2875=
XM_017009188.1:c.7960T=	XP_016864677.1:p.Ter2654=
XM_024454388.1:c.12886T=	XP_024310156.1:p.Ter4296=
XM_024454389.1:c.12475T=	XP_024310157.1:p.Ter4159=
NM_001369.3:c.13873T= MANE Select	NP_001360.1:p.Ter4625=