Canonical Allele Identifier: CA443535962

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13753591A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753482A>G , CM000667.2:g.13753482A>G	GRCh38
NC_000005.9:g.13753591A>G , CM000667.1:g.13753591A>G	GRCh37
NC_000005.8:g.13806591A>G	NCBI36
NG_013081.1:g.195999T>C
NG_013081.2:g.195999T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10623T>C MANE Select	ENSP00000265104.4:p.Leu3541=
ENST00000681290.1:c.10578T>C	ENSP00000505288.1:p.Leu3526=
ENST00000265104.4:c.10623T>C	ENSP00000265104.4:p.Leu3541=
NM_001369.2:c.10623T>C	NP_001360.1:p.Leu3541=
XM_005248262.2:c.10578T>C	XP_005248319.1:p.Leu3526=
XM_005248262.3:c.10731T>C	XP_005248319.2:p.Leu3577=
XM_017009177.1:c.10731T>C	XP_016864666.1:p.Leu3577=
XM_017009178.1:c.9636T>C	XP_016864667.1:p.Leu3212=
XM_017009179.2:c.9636T>C	XP_016864668.1:p.Leu3212=
XM_017009180.1:c.10731T>C	XP_016864669.1:p.Leu3577=
XM_017009181.1:c.10731T>C	XP_016864670.1:p.Leu3577=
XM_017009182.1:c.10731T>C	XP_016864671.1:p.Leu3577=
XM_017009185.1:c.5820T>C	XP_016864674.1:p.Leu1940=
XM_017009186.1:c.5373T>C	XP_016864675.1:p.Leu1791=
XM_017009188.1:c.4710T>C	XP_016864677.1:p.Leu1570=
XM_024454388.1:c.9636T>C	XP_024310156.1:p.Leu3212=
XM_024454389.1:c.9225T>C	XP_024310157.1:p.Leu3075=
NM_001369.3:c.10623T>C MANE Select	NP_001360.1:p.Leu3541=