Canonical Allele Identifier: CA1528395859

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13692052G= , CM000667.2:g.13692052G=	GRCh38
NC_000005.9:g.13692161G= , CM000667.1:g.13692161G=	GRCh37
NC_000005.8:g.13745161G=	NCBI36
NG_013081.1:g.257429C=
NG_013081.2:g.257429C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1140C=
ENST00000265104.5:c.13807C= MANE Select	ENSP00000265104.4:p.Leu4603=
ENST00000681290.1:c.13762C=	ENSP00000505288.1:p.Leu4588=
ENST00000265104.4:c.13807C=	ENSP00000265104.4:p.Leu4603=
NM_001369.2:c.13807C=	NP_001360.1:p.Leu4603=
XM_005248262.2:c.13762C=	XP_005248319.1:p.Leu4588=
XM_005248262.3:c.13915C=	XP_005248319.2:p.Leu4639=
XM_017009177.1:c.13495C=	XP_016864666.1:p.Leu4499=
XM_017009178.1:c.12820C=	XP_016864667.1:p.Leu4274=
XM_017009179.2:c.12820C=	XP_016864668.1:p.Leu4274=
XM_017009185.1:c.9004C=	XP_016864674.1:p.Leu3002=
XM_017009186.1:c.8557C=	XP_016864675.1:p.Leu2853=
XM_017009188.1:c.7894C=	XP_016864677.1:p.Leu2632=
XM_024454388.1:c.12820C=	XP_024310156.1:p.Leu4274=
XM_024454389.1:c.12409C=	XP_024310157.1:p.Leu4137=
NM_001369.3:c.13807C= MANE Select	NP_001360.1:p.Leu4603=