Canonical Allele Identifier: CA1528395891

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13692123G= , CM000667.2:g.13692123G=	GRCh38
NC_000005.9:g.13692232G= , CM000667.1:g.13692232G=	GRCh37
NC_000005.8:g.13745232G=	NCBI36
NG_013081.1:g.257358C=
NG_013081.2:g.257358C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1069C=
ENST00000265104.5:c.13736C= MANE Select	ENSP00000265104.4:p.Pro4579=
ENST00000681290.1:c.13691C=	ENSP00000505288.1:p.Pro4564=
ENST00000265104.4:c.13736C=	ENSP00000265104.4:p.Pro4579=
NM_001369.2:c.13736C=	NP_001360.1:p.Pro4579=
XM_005248262.2:c.13691C=	XP_005248319.1:p.Pro4564=
XM_005248262.3:c.13844C=	XP_005248319.2:p.Pro4615=
XM_017009177.1:c.13424C=	XP_016864666.1:p.Pro4475=
XM_017009178.1:c.12749C=	XP_016864667.1:p.Pro4250=
XM_017009179.2:c.12749C=	XP_016864668.1:p.Pro4250=
XM_017009185.1:c.8933C=	XP_016864674.1:p.Pro2978=
XM_017009186.1:c.8486C=	XP_016864675.1:p.Pro2829=
XM_017009188.1:c.7823C=	XP_016864677.1:p.Pro2608=
XM_024454388.1:c.12749C=	XP_024310156.1:p.Pro4250=
XM_024454389.1:c.12338C=	XP_024310157.1:p.Pro4113=
NM_001369.3:c.13736C= MANE Select	NP_001360.1:p.Pro4579=