Canonical Allele Identifier: CA359191766

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13753526A>C (hg19) ; chr5:g.13753417A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753417A>C , CM000667.2:g.13753417A>C	GRCh38
NC_000005.9:g.13753526A>C , CM000667.1:g.13753526A>C	GRCh37
NC_000005.8:g.13806526A>C	NCBI36
NG_013081.1:g.196064T>G
NG_013081.2:g.196064T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10688T>G MANE Select	ENSP00000265104.4:p.Leu3563Arg
ENST00000681290.1:c.10643T>G	ENSP00000505288.1:p.Leu3548Arg
ENST00000265104.4:c.10688T>G	ENSP00000265104.4:p.Leu3563Arg
NM_001369.2:c.10688T>G	NP_001360.1:p.Leu3563Arg
XM_005248262.2:c.10643T>G	XP_005248319.1:p.Leu3548Arg
XM_005248262.3:c.10796T>G	XP_005248319.2:p.Leu3599Arg
XM_017009177.1:c.10796T>G	XP_016864666.1:p.Leu3599Arg
XM_017009178.1:c.9701T>G	XP_016864667.1:p.Leu3234Arg
XM_017009179.2:c.9701T>G	XP_016864668.1:p.Leu3234Arg
XM_017009180.1:c.10796T>G	XP_016864669.1:p.Leu3599Arg
XM_017009181.1:c.10796T>G	XP_016864670.1:p.Leu3599Arg
XM_017009182.1:c.10796T>G	XP_016864671.1:p.Leu3599Arg
XM_017009185.1:c.5885T>G	XP_016864674.1:p.Leu1962Arg
XM_017009186.1:c.5438T>G	XP_016864675.1:p.Leu1813Arg
XM_017009188.1:c.4775T>G	XP_016864677.1:p.Leu1592Arg
XM_024454388.1:c.9701T>G	XP_024310156.1:p.Leu3234Arg
XM_024454389.1:c.9290T>G	XP_024310157.1:p.Leu3097Arg
NM_001369.3:c.10688T>G MANE Select	NP_001360.1:p.Leu3563Arg