Canonical Allele Identifier: CA359209239

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13776730A>C (hg19) ; chr5:g.13776621A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776621A>C , CM000667.2:g.13776621A>C	GRCh38
NC_000005.9:g.13776730A>C , CM000667.1:g.13776730A>C	GRCh37
NC_000005.8:g.13829730A>C	NCBI36
NG_013081.1:g.172860T>G
NG_013081.2:g.172860T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9191T>G MANE Select	ENSP00000265104.4:p.Leu3064Arg
ENST00000681290.1:c.9146T>G	ENSP00000505288.1:p.Leu3049Arg
ENST00000265104.4:c.9191T>G	ENSP00000265104.4:p.Leu3064Arg
NM_001369.2:c.9191T>G	NP_001360.1:p.Leu3064Arg
XM_005248262.2:c.9146T>G	XP_005248319.1:p.Leu3049Arg
XM_005248262.3:c.9299T>G	XP_005248319.2:p.Leu3100Arg
XM_017009177.1:c.9299T>G	XP_016864666.1:p.Leu3100Arg
XM_017009178.1:c.8204T>G	XP_016864667.1:p.Leu2735Arg
XM_017009179.2:c.8204T>G	XP_016864668.1:p.Leu2735Arg
XM_017009180.1:c.9299T>G	XP_016864669.1:p.Leu3100Arg
XM_017009181.1:c.9299T>G	XP_016864670.1:p.Leu3100Arg
XM_017009182.1:c.9299T>G	XP_016864671.1:p.Leu3100Arg
XM_017009183.1:c.9299T>G	XP_016864672.1:p.Leu3100Arg
XM_017009185.1:c.4388T>G	XP_016864674.1:p.Leu1463Arg
XM_017009186.1:c.3941T>G	XP_016864675.1:p.Leu1314Arg
XM_017009188.1:c.3278T>G	XP_016864677.1:p.Leu1093Arg
XM_024454388.1:c.8204T>G	XP_024310156.1:p.Leu2735Arg
XM_024454389.1:c.7793T>G	XP_024310157.1:p.Leu2598Arg
XR_001742034.1:n.9185T>G
NM_001369.3:c.9191T>G MANE Select	NP_001360.1:p.Leu3064Arg