Canonical Allele Identifier: CA1528395893

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13692125A= , CM000667.2:g.13692125A=	GRCh38
NC_000005.9:g.13692234A= , CM000667.1:g.13692234A=	GRCh37
NC_000005.8:g.13745234A=	NCBI36
NG_013081.1:g.257356T=
NG_013081.2:g.257356T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1067T=
ENST00000265104.5:c.13734T= MANE Select	ENSP00000265104.4:p.Asp4578=
ENST00000681290.1:c.13689T=	ENSP00000505288.1:p.Asp4563=
ENST00000265104.4:c.13734T=	ENSP00000265104.4:p.Asp4578=
NM_001369.2:c.13734T=	NP_001360.1:p.Asp4578=
XM_005248262.2:c.13689T=	XP_005248319.1:p.Asp4563=
XM_005248262.3:c.13842T=	XP_005248319.2:p.Asp4614=
XM_017009177.1:c.13422T=	XP_016864666.1:p.Asp4474=
XM_017009178.1:c.12747T=	XP_016864667.1:p.Asp4249=
XM_017009179.2:c.12747T=	XP_016864668.1:p.Asp4249=
XM_017009185.1:c.8931T=	XP_016864674.1:p.Asp2977=
XM_017009186.1:c.8484T=	XP_016864675.1:p.Asp2828=
XM_017009188.1:c.7821T=	XP_016864677.1:p.Asp2607=
XM_024454388.1:c.12747T=	XP_024310156.1:p.Asp4249=
XM_024454389.1:c.12336T=	XP_024310157.1:p.Asp4112=
NM_001369.3:c.13734T= MANE Select	NP_001360.1:p.Asp4578=