Canonical Allele Identifier: CA359221825

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13794063G>C (hg19) ; chr5:g.13793954G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793954G>C , CM000667.2:g.13793954G>C	GRCh38
NC_000005.9:g.13794063G>C , CM000667.1:g.13794063G>C	GRCh37
NC_000005.8:g.13847063G>C	NCBI36
NG_013081.1:g.155527C>G
NG_013081.2:g.155527C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.7992C>G MANE Select	ENSP00000265104.4:p.Ile2664Met
ENST00000681290.1:c.7947C>G	ENSP00000505288.1:p.Ile2649Met
ENST00000265104.4:c.7992C>G	ENSP00000265104.4:p.Ile2664Met
NM_001369.2:c.7992C>G	NP_001360.1:p.Ile2664Met
XM_005248262.2:c.7947C>G	XP_005248319.1:p.Ile2649Met
XM_011513990.1:c.7992C>G	XP_011512292.1:p.Ile2664Met
XR_925598.1:n.8199C>G
XM_005248262.3:c.8100C>G	XP_005248319.2:p.Ile2700Met
XM_017009177.1:c.8100C>G	XP_016864666.1:p.Ile2700Met
XM_017009178.1:c.7005C>G	XP_016864667.1:p.Ile2335Met
XM_017009179.2:c.7005C>G	XP_016864668.1:p.Ile2335Met
XM_017009180.1:c.8100C>G	XP_016864669.1:p.Ile2700Met
XM_017009181.1:c.8100C>G	XP_016864670.1:p.Ile2700Met
XM_017009182.1:c.8100C>G	XP_016864671.1:p.Ile2700Met
XM_017009183.1:c.8100C>G	XP_016864672.1:p.Ile2700Met
XM_017009184.1:c.8100C>G	XP_016864673.1:p.Ile2700Met
XM_017009185.1:c.3189C>G	XP_016864674.1:p.Ile1063Met
XM_017009186.1:c.2742C>G	XP_016864675.1:p.Ile914Met
XM_017009188.1:c.2079C>G	XP_016864677.1:p.Ile693Met
XM_024454388.1:c.7005C>G	XP_024310156.1:p.Ile2335Met
XM_024454389.1:c.6594C>G	XP_024310157.1:p.Ile2198Met
XR_001742034.1:n.8117C>G
XR_001742035.1:n.8117C>G
NM_001369.3:c.7992C>G MANE Select	NP_001360.1:p.Ile2664Met