Canonical Allele Identifier: CA359204931

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13771008A>C (hg19) ; chr5:g.13770899A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13770899A>C , CM000667.2:g.13770899A>C	GRCh38
NC_000005.9:g.13771008A>C , CM000667.1:g.13771008A>C	GRCh37
NC_000005.8:g.13824008A>C	NCBI36
NG_013081.1:g.178582T>G
NG_013081.2:g.178582T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9455T>G MANE Select	ENSP00000265104.4:p.Phe3152Cys
ENST00000681290.1:c.9410T>G	ENSP00000505288.1:p.Phe3137Cys
ENST00000265104.4:c.9455T>G	ENSP00000265104.4:p.Phe3152Cys
ENST00000504001.3:n.167T>G
NM_001369.2:c.9455T>G	NP_001360.1:p.Phe3152Cys
XM_005248262.2:c.9410T>G	XP_005248319.1:p.Phe3137Cys
XM_005248262.3:c.9563T>G	XP_005248319.2:p.Phe3188Cys
XM_017009177.1:c.9563T>G	XP_016864666.1:p.Phe3188Cys
XM_017009178.1:c.8468T>G	XP_016864667.1:p.Phe2823Cys
XM_017009179.2:c.8468T>G	XP_016864668.1:p.Phe2823Cys
XM_017009180.1:c.9563T>G	XP_016864669.1:p.Phe3188Cys
XM_017009181.1:c.9563T>G	XP_016864670.1:p.Phe3188Cys
XM_017009182.1:c.9563T>G	XP_016864671.1:p.Phe3188Cys
XM_017009183.1:c.9563T>G	XP_016864672.1:p.Phe3188Cys
XM_017009185.1:c.4652T>G	XP_016864674.1:p.Phe1551Cys
XM_017009186.1:c.4205T>G	XP_016864675.1:p.Phe1402Cys
XM_017009188.1:c.3542T>G	XP_016864677.1:p.Phe1181Cys
XM_024454388.1:c.8468T>G	XP_024310156.1:p.Phe2823Cys
XM_024454389.1:c.8057T>G	XP_024310157.1:p.Phe2686Cys
NM_001369.3:c.9455T>G MANE Select	NP_001360.1:p.Phe3152Cys