Canonical Allele Identifier: CA359211715

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13911403G>A , CM000667.2:g.13911403G>A	GRCh38
NC_000005.9:g.13911512G>A , CM000667.1:g.13911512G>A	GRCh37
NC_000005.8:g.13964512G>A	NCBI36
NG_013081.1:g.38078C>T
NG_013081.2:g.38078C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.1627C>T MANE Select	NP_001360.1:p.Gln543Ter
ENST00000265104.5:c.1627C>T MANE Select	ENSP00000265104.4:p.Gln543Ter
NM_001369.2:c.1627C>T	NP_001360.1:p.Gln543Ter
ENST00000265104.4:c.1627C>T	ENSP00000265104.4:p.Gln543Ter
ENST00000508040.1:n.2035C>T
ENST00000680213.1:c.1387C>T	ENSP00000506622.1:p.Gln463Ter
ENST00000680213.2:n.1683C>T
ENST00000681290.1:c.1582C>T	ENSP00000505288.1:p.Gln528Ter
ENST00000683011.1:n.1566C>T
ENST00000683967.1:n.3992C>T
ENST00000684013.1:n.2287C>T
ENST00000684099.1:n.2283C>T
XM_005248262.2:c.1582C>T	XP_005248319.1:p.Gln528Ter
XM_005248262.3:c.1735C>T	XP_005248319.2:p.Gln579Ter
XM_011513990.1:c.1627C>T	XP_011512292.1:p.Gln543Ter
XM_017009177.1:c.1735C>T	XP_016864666.1:p.Gln579Ter
XM_017009178.1:c.640C>T	XP_016864667.1:p.Gln214Ter
XM_017009179.2:c.640C>T	XP_016864668.1:p.Gln214Ter
XM_017009180.1:c.1735C>T	XP_016864669.1:p.Gln579Ter
XM_017009181.1:c.1735C>T	XP_016864670.1:p.Gln579Ter
XM_017009182.1:c.1735C>T	XP_016864671.1:p.Gln579Ter
XM_017009183.1:c.1735C>T	XP_016864672.1:p.Gln579Ter
XM_017009184.1:c.1735C>T	XP_016864673.1:p.Gln579Ter
XM_017009187.1:c.1735C>T	XP_016864676.1:p.Gln579Ter
XM_024454388.1:c.640C>T	XP_024310156.1:p.Gln214Ter
XM_024454389.1:c.229C>T	XP_024310157.1:p.Gln77Ter
XR_001742034.1:n.1752C>T
XR_001742035.1:n.1752C>T
XR_925598.1:n.1834C>T