Canonical Allele Identifier: CA359225152

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13736015A>C (hg19) ; chr5:g.13735906A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13735906A>C , CM000667.2:g.13735906A>C	GRCh38
NC_000005.9:g.13736015A>C , CM000667.1:g.13736015A>C	GRCh37
NC_000005.8:g.13789015A>C	NCBI36
NG_013081.1:g.213575T>G
NG_013081.2:g.213575T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.11482T>G MANE Select	ENSP00000265104.4:p.Phe3828Val
ENST00000681290.1:c.11437T>G	ENSP00000505288.1:p.Phe3813Val
ENST00000265104.4:c.11482T>G	ENSP00000265104.4:p.Phe3828Val
NM_001369.2:c.11482T>G	NP_001360.1:p.Phe3828Val
XM_005248262.2:c.11437T>G	XP_005248319.1:p.Phe3813Val
XM_005248262.3:c.11590T>G	XP_005248319.2:p.Phe3864Val
XM_017009177.1:c.11590T>G	XP_016864666.1:p.Phe3864Val
XM_017009178.1:c.10495T>G	XP_016864667.1:p.Phe3499Val
XM_017009179.2:c.10495T>G	XP_016864668.1:p.Phe3499Val
XM_017009180.1:c.11590T>G	XP_016864669.1:p.Phe3864Val
XM_017009181.1:c.11590T>G	XP_016864670.1:p.Phe3864Val
XM_017009182.1:c.11346T>G	XP_016864671.1:p.Thr3782=
XM_017009185.1:c.6679T>G	XP_016864674.1:p.Phe2227Val
XM_017009186.1:c.6232T>G	XP_016864675.1:p.Phe2078Val
XM_017009188.1:c.5569T>G	XP_016864677.1:p.Phe1857Val
XM_024454388.1:c.10495T>G	XP_024310156.1:p.Phe3499Val
XM_024454389.1:c.10084T>G	XP_024310157.1:p.Phe3362Val
NM_001369.3:c.11482T>G MANE Select	NP_001360.1:p.Phe3828Val