Canonical Allele Identifier: CA443248589

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13752146C>A , CM000667.2:g.13752146C>A	GRCh38
NC_000005.9:g.13752255C>A , CM000667.1:g.13752255C>A	GRCh37
NC_000005.8:g.13805255C>A	NCBI36
NG_013081.1:g.197335G>T
NG_013081.2:g.197335G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.11016G>T MANE Select	NP_001360.1:p.Gly3672=
ENST00000265104.5:c.11016G>T MANE Select	ENSP00000265104.4:p.Gly3672=
NM_001369.2:c.11016G>T	NP_001360.1:p.Gly3672=
ENST00000265104.4:c.11016G>T	ENSP00000265104.4:p.Gly3672=
ENST00000681290.1:c.10971G>T	ENSP00000505288.1:p.Gly3657=
XM_005248262.2:c.10971G>T	XP_005248319.1:p.Gly3657=
XM_005248262.3:c.11124G>T	XP_005248319.2:p.Gly3708=
XM_017009177.1:c.11124G>T	XP_016864666.1:p.Gly3708=
XM_017009178.1:c.10029G>T	XP_016864667.1:p.Gly3343=
XM_017009179.2:c.10029G>T	XP_016864668.1:p.Gly3343=
XM_017009180.1:c.11124G>T	XP_016864669.1:p.Gly3708=
XM_017009181.1:c.11124G>T	XP_016864670.1:p.Gly3708=
XM_017009182.1:c.11124G>T	XP_016864671.1:p.Gly3708=
XM_017009185.1:c.6213G>T	XP_016864674.1:p.Gly2071=
XM_017009186.1:c.5766G>T	XP_016864675.1:p.Gly1922=
XM_017009188.1:c.5103G>T	XP_016864677.1:p.Gly1701=
XM_024454388.1:c.10029G>T	XP_024310156.1:p.Gly3343=
XM_024454389.1:c.9618G>T	XP_024310157.1:p.Gly3206=