Canonical Allele Identifier: CA3203037

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13809165G>A , CM000667.2:g.13809165G>A	GRCh38
NC_000005.9:g.13809274G>A , CM000667.1:g.13809274G>A	GRCh37
NC_000005.8:g.13862274G>A	NCBI36
NG_013081.1:g.140316C>T
NG_013081.2:g.140316C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.7631C>T MANE Select	NP_001360.1:p.Thr2544Met
ENST00000265104.5:c.7631C>T MANE Select	ENSP00000265104.4:p.Thr2544Met
NM_001369.2:c.7631C>T	NP_001360.1:p.Thr2544Met
ENST00000265104.4:c.7631C>T	ENSP00000265104.4:p.Thr2544Met
ENST00000512443.1:n.487C>T
ENST00000681290.1:c.7586C>T	ENSP00000505288.1:p.Thr2529Met
XM_005248262.2:c.7586C>T	XP_005248319.1:p.Thr2529Met
XM_005248262.3:c.7739C>T	XP_005248319.2:p.Thr2580Met
XM_011513990.1:c.7631C>T	XP_011512292.1:p.Thr2544Met
XM_017009177.1:c.7739C>T	XP_016864666.1:p.Thr2580Met
XM_017009178.1:c.6644C>T	XP_016864667.1:p.Thr2215Met
XM_017009179.2:c.6644C>T	XP_016864668.1:p.Thr2215Met
XM_017009180.1:c.7739C>T	XP_016864669.1:p.Thr2580Met
XM_017009181.1:c.7739C>T	XP_016864670.1:p.Thr2580Met
XM_017009182.1:c.7739C>T	XP_016864671.1:p.Thr2580Met
XM_017009183.1:c.7739C>T	XP_016864672.1:p.Thr2580Met
XM_017009184.1:c.7739C>T	XP_016864673.1:p.Thr2580Met
XM_017009185.1:c.2828C>T	XP_016864674.1:p.Thr943Met
XM_017009186.1:c.2381C>T	XP_016864675.1:p.Thr794Met
XM_017009187.1:c.7739C>T	XP_016864676.1:p.Thr2580Met
XM_017009188.1:c.1718C>T	XP_016864677.1:p.Thr573Met
XM_024454388.1:c.6644C>T	XP_024310156.1:p.Thr2215Met
XM_024454389.1:c.6233C>T	XP_024310157.1:p.Thr2078Met
XR_001742034.1:n.7756C>T
XR_001742035.1:n.7756C>T
XR_925598.1:n.7838C>T