Canonical Allele Identifier: CA359225371

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13736041A>T (hg19) ; chr5:g.13735932A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13735932A>T , CM000667.2:g.13735932A>T	GRCh38
NC_000005.9:g.13736041A>T , CM000667.1:g.13736041A>T	GRCh37
NC_000005.8:g.13789041A>T	NCBI36
NG_013081.1:g.213549T>A
NG_013081.2:g.213549T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.11456T>A MANE Select	ENSP00000265104.4:p.Val3819Glu
ENST00000681290.1:c.11411T>A	ENSP00000505288.1:p.Val3804Glu
ENST00000265104.4:c.11456T>A	ENSP00000265104.4:p.Val3819Glu
NM_001369.2:c.11456T>A	NP_001360.1:p.Val3819Glu
XM_005248262.2:c.11411T>A	XP_005248319.1:p.Val3804Glu
XM_005248262.3:c.11564T>A	XP_005248319.2:p.Val3855Glu
XM_017009177.1:c.11564T>A	XP_016864666.1:p.Val3855Glu
XM_017009178.1:c.10469T>A	XP_016864667.1:p.Val3490Glu
XM_017009179.2:c.10469T>A	XP_016864668.1:p.Val3490Glu
XM_017009180.1:c.11564T>A	XP_016864669.1:p.Val3855Glu
XM_017009181.1:c.11564T>A	XP_016864670.1:p.Val3855Glu
XM_017009182.1:c.11320T>A	XP_016864671.1:p.Trp3774Arg
XM_017009185.1:c.6653T>A	XP_016864674.1:p.Val2218Glu
XM_017009186.1:c.6206T>A	XP_016864675.1:p.Val2069Glu
XM_017009188.1:c.5543T>A	XP_016864677.1:p.Val1848Glu
XM_024454388.1:c.10469T>A	XP_024310156.1:p.Val3490Glu
XM_024454389.1:c.10058T>A	XP_024310157.1:p.Val3353Glu
NM_001369.3:c.11456T>A MANE Select	NP_001360.1:p.Val3819Glu