Canonical Allele Identifier: CA1528395881

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13692106G= , CM000667.2:g.13692106G=	GRCh38
NC_000005.9:g.13692215G= , CM000667.1:g.13692215G=	GRCh37
NC_000005.8:g.13745215G=	NCBI36
NG_013081.1:g.257375C=
NG_013081.2:g.257375C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1086C=
ENST00000265104.5:c.13753C= MANE Select	ENSP00000265104.4:p.Pro4585=
ENST00000681290.1:c.13708C=	ENSP00000505288.1:p.Pro4570=
ENST00000265104.4:c.13753C=	ENSP00000265104.4:p.Pro4585=
NM_001369.2:c.13753C=	NP_001360.1:p.Pro4585=
XM_005248262.2:c.13708C=	XP_005248319.1:p.Pro4570=
XM_005248262.3:c.13861C=	XP_005248319.2:p.Pro4621=
XM_017009177.1:c.13441C=	XP_016864666.1:p.Pro4481=
XM_017009178.1:c.12766C=	XP_016864667.1:p.Pro4256=
XM_017009179.2:c.12766C=	XP_016864668.1:p.Pro4256=
XM_017009185.1:c.8950C=	XP_016864674.1:p.Pro2984=
XM_017009186.1:c.8503C=	XP_016864675.1:p.Pro2835=
XM_017009188.1:c.7840C=	XP_016864677.1:p.Pro2614=
XM_024454388.1:c.12766C=	XP_024310156.1:p.Pro4256=
XM_024454389.1:c.12355C=	XP_024310157.1:p.Pro4119=
NM_001369.3:c.13753C= MANE Select	NP_001360.1:p.Pro4585=