Canonical Allele Identifier: CA3204872

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13913944G>A , CM000667.2:g.13913944G>A	GRCh38
NC_000005.9:g.13914053G>A , CM000667.1:g.13914053G>A	GRCh37
NC_000005.8:g.13967053G>A	NCBI36
NG_013081.1:g.35537C>T
NG_013081.2:g.35537C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.1335C>T MANE Select	NP_001360.1:p.Cys445=
ENST00000265104.5:c.1335C>T MANE Select	ENSP00000265104.4:p.Cys445=
NM_001369.2:c.1335C>T	NP_001360.1:p.Cys445=
ENST00000265104.4:c.1335C>T	ENSP00000265104.4:p.Cys445=
ENST00000508040.1:n.1743C>T
ENST00000680213.1:c.1095C>T	ENSP00000506622.1:p.Cys365=
ENST00000680213.2:n.1391C>T
ENST00000681290.1:c.1290C>T	ENSP00000505288.1:p.Cys430=
ENST00000682376.1:n.5564C>T
ENST00000683011.1:n.1274C>T
ENST00000683967.1:n.3700C>T
ENST00000684013.1:n.1995C>T
ENST00000684099.1:n.1991C>T
XM_005248262.2:c.1290C>T	XP_005248319.1:p.Cys430=
XM_005248262.3:c.1443C>T	XP_005248319.2:p.Cys481=
XM_011513990.1:c.1335C>T	XP_011512292.1:p.Cys445=
XM_017009177.1:c.1443C>T	XP_016864666.1:p.Cys481=
XM_017009178.1:c.348C>T	XP_016864667.1:p.Cys116=
XM_017009179.2:c.348C>T	XP_016864668.1:p.Cys116=
XM_017009180.1:c.1443C>T	XP_016864669.1:p.Cys481=
XM_017009181.1:c.1443C>T	XP_016864670.1:p.Cys481=
XM_017009182.1:c.1443C>T	XP_016864671.1:p.Cys481=
XM_017009183.1:c.1443C>T	XP_016864672.1:p.Cys481=
XM_017009184.1:c.1443C>T	XP_016864673.1:p.Cys481=
XM_017009187.1:c.1443C>T	XP_016864676.1:p.Cys481=
XM_024454388.1:c.348C>T	XP_024310156.1:p.Cys116=
XM_024454389.1:c.-64C>T	XP_024310157.1:n.-64C>T
XR_001742034.1:n.1460C>T
XR_001742035.1:n.1460C>T
XR_925598.1:n.1542C>T