Canonical Allele Identifier: CA1528395851

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13692027T= , CM000667.2:g.13692027T=	GRCh38
NC_000005.9:g.13692136T= , CM000667.1:g.13692136T=	GRCh37
NC_000005.8:g.13745136T=	NCBI36
NG_013081.1:g.257454A=
NG_013081.2:g.257454A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1165A=
ENST00000265104.5:c.13832A= MANE Select	ENSP00000265104.4:p.His4611=
ENST00000681290.1:c.13787A=	ENSP00000505288.1:p.His4596=
ENST00000265104.4:c.13832A=	ENSP00000265104.4:p.His4611=
NM_001369.2:c.13832A=	NP_001360.1:p.His4611=
XM_005248262.2:c.13787A=	XP_005248319.1:p.His4596=
XM_005248262.3:c.13940A=	XP_005248319.2:p.His4647=
XM_017009177.1:c.13520A=	XP_016864666.1:p.His4507=
XM_017009178.1:c.12845A=	XP_016864667.1:p.His4282=
XM_017009179.2:c.12845A=	XP_016864668.1:p.His4282=
XM_017009185.1:c.9029A=	XP_016864674.1:p.His3010=
XM_017009186.1:c.8582A=	XP_016864675.1:p.His2861=
XM_017009188.1:c.7919A=	XP_016864677.1:p.His2640=
XM_024454388.1:c.12845A=	XP_024310156.1:p.His4282=
XM_024454389.1:c.12434A=	XP_024310157.1:p.His4145=
NM_001369.3:c.13832A= MANE Select	NP_001360.1:p.His4611=