Canonical Allele Identifier: CA1528403759

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708197T= , CM000667.2:g.13708197T=	GRCh38
NC_000005.9:g.13708306T= , CM000667.1:g.13708306T=	GRCh37
NC_000005.8:g.13761306T=	NCBI36
NG_013081.1:g.241284A=
NG_013081.2:g.241284A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.597A=
ENST00000265104.5:c.13264A= MANE Select	ENSP00000265104.4:p.Ile4422=
ENST00000681290.1:c.13219A=	ENSP00000505288.1:p.Ile4407=
ENST00000265104.4:c.13264A=	ENSP00000265104.4:p.Ile4422=
NM_001369.2:c.13264A=	NP_001360.1:p.Ile4422=
XM_005248262.2:c.13219A=	XP_005248319.1:p.Ile4407=
XM_005248262.3:c.13372A=	XP_005248319.2:p.Ile4458=
XM_017009177.1:c.12952A=	XP_016864666.1:p.Ile4318=
XM_017009178.1:c.12277A=	XP_016864667.1:p.Ile4093=
XM_017009179.2:c.12277A=	XP_016864668.1:p.Ile4093=
XM_017009185.1:c.8461A=	XP_016864674.1:p.Ile2821=
XM_017009186.1:c.8014A=	XP_016864675.1:p.Ile2672=
XM_017009188.1:c.7351A=	XP_016864677.1:p.Ile2451=
XM_024454388.1:c.12277A=	XP_024310156.1:p.Ile4093=
XM_024454389.1:c.11866A=	XP_024310157.1:p.Ile3956=
NM_001369.3:c.13264A= MANE Select	NP_001360.1:p.Ile4422=