Canonical Allele Identifier: CA359224993

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13736002T>C (hg19) ; chr5:g.13735893T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13735893T>C , CM000667.2:g.13735893T>C	GRCh38
NC_000005.9:g.13736002T>C , CM000667.1:g.13736002T>C	GRCh37
NC_000005.8:g.13789002T>C	NCBI36
NG_013081.1:g.213588A>G
NG_013081.2:g.213588A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.11495A>G MANE Select	ENSP00000265104.4:p.Glu3832Gly
ENST00000681290.1:c.11450A>G	ENSP00000505288.1:p.Glu3817Gly
ENST00000265104.4:c.11495A>G	ENSP00000265104.4:p.Glu3832Gly
NM_001369.2:c.11495A>G	NP_001360.1:p.Glu3832Gly
XM_005248262.2:c.11450A>G	XP_005248319.1:p.Glu3817Gly
XM_005248262.3:c.11603A>G	XP_005248319.2:p.Glu3868Gly
XM_017009177.1:c.11603A>G	XP_016864666.1:p.Glu3868Gly
XM_017009178.1:c.10508A>G	XP_016864667.1:p.Glu3503Gly
XM_017009179.2:c.10508A>G	XP_016864668.1:p.Glu3503Gly
XM_017009180.1:c.11603A>G	XP_016864669.1:p.Glu3868Gly
XM_017009181.1:c.11603A>G	XP_016864670.1:p.Glu3868Gly
XM_017009182.1:c.11359A>G	XP_016864671.1:p.Arg3787Gly
XM_017009185.1:c.6692A>G	XP_016864674.1:p.Glu2231Gly
XM_017009186.1:c.6245A>G	XP_016864675.1:p.Glu2082Gly
XM_017009188.1:c.5582A>G	XP_016864677.1:p.Glu1861Gly
XM_024454388.1:c.10508A>G	XP_024310156.1:p.Glu3503Gly
XM_024454389.1:c.10097A>G	XP_024310157.1:p.Glu3366Gly
NM_001369.3:c.11495A>G MANE Select	NP_001360.1:p.Glu3832Gly