Canonical Allele Identifier: CA3205169

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13922291C>A , CM000667.2:g.13922291C>A	GRCh38
NC_000005.9:g.13922400C>A , CM000667.1:g.13922400C>A	GRCh37
NC_000005.8:g.13975400C>A	NCBI36
NG_013081.1:g.27190G>T
NG_013081.2:g.27190G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.476G>T MANE Select	NP_001360.1:p.Gly159Val
ENST00000265104.5:c.476G>T MANE Select	ENSP00000265104.4:p.Gly159Val
NM_001369.2:c.476G>T	NP_001360.1:p.Gly159Val
ENST00000265104.4:c.476G>T	ENSP00000265104.4:p.Gly159Val
ENST00000508040.1:n.835G>T
ENST00000680213.1:c.236G>T	ENSP00000506622.1:p.Gly79Val
ENST00000680213.2:n.532G>T
ENST00000681290.1:c.431G>T	ENSP00000505288.1:p.Gly144Val
ENST00000682376.1:n.520G>T
ENST00000682586.1:n.520G>T
ENST00000683011.1:n.415G>T
ENST00000683967.1:n.526G>T
ENST00000684013.1:n.526G>T
ENST00000684099.1:n.571G>T
XM_005248262.2:c.431G>T	XP_005248319.1:p.Gly144Val
XM_005248262.3:c.584G>T	XP_005248319.2:p.Gly195Val
XM_011513990.1:c.476G>T	XP_011512292.1:p.Gly159Val
XM_017009177.1:c.584G>T	XP_016864666.1:p.Gly195Val
XM_017009178.1:c.-561G>T	XP_016864667.1:n.-561G>T
XM_017009180.1:c.584G>T	XP_016864669.1:p.Gly195Val
XM_017009181.1:c.584G>T	XP_016864670.1:p.Gly195Val
XM_017009182.1:c.584G>T	XP_016864671.1:p.Gly195Val
XM_017009183.1:c.584G>T	XP_016864672.1:p.Gly195Val
XM_017009184.1:c.584G>T	XP_016864673.1:p.Gly195Val
XM_017009187.1:c.584G>T	XP_016864676.1:p.Gly195Val
XM_024454388.1:c.-2431G>T	XP_024310156.1:n.-2431G>T
XM_024454389.1:c.-1484G>T	XP_024310157.1:n.-1484G>T
XR_001742034.1:n.601G>T
XR_001742035.1:n.601G>T
XR_925598.1:n.683G>T