Canonical Allele Identifier: CA359218277

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13727599C>A , CM000667.2:g.13727599C>A	GRCh38
NC_000005.9:g.13727708C>A , CM000667.1:g.13727708C>A	GRCh37
NC_000005.8:g.13780708C>A	NCBI36
NG_013081.1:g.221882G>T
NG_013081.2:g.221882G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.11941G>T MANE Select	NP_001360.1:p.Glu3981Ter
ENST00000265104.5:c.11941G>T MANE Select	ENSP00000265104.4:p.Glu3981Ter
NM_001369.2:c.11941G>T	NP_001360.1:p.Glu3981Ter
ENST00000265104.4:c.11941G>T	ENSP00000265104.4:p.Glu3981Ter
ENST00000681290.1:c.11896G>T	ENSP00000505288.1:p.Glu3966Ter
XM_005248262.2:c.11896G>T	XP_005248319.1:p.Glu3966Ter
XM_005248262.3:c.12049G>T	XP_005248319.2:p.Glu4017Ter
XM_017009177.1:c.12049G>T	XP_016864666.1:p.Glu4017Ter
XM_017009178.1:c.10954G>T	XP_016864667.1:p.Glu3652Ter
XM_017009179.2:c.10954G>T	XP_016864668.1:p.Glu3652Ter
XM_017009180.1:c.12049G>T	XP_016864669.1:p.Glu4017Ter
XM_017009181.1:c.*44G>T	XP_016864670.1:n.*44G>T
XM_017009185.1:c.7138G>T	XP_016864674.1:p.Glu2380Ter
XM_017009186.1:c.6691G>T	XP_016864675.1:p.Glu2231Ter
XM_017009188.1:c.6028G>T	XP_016864677.1:p.Glu2010Ter
XM_024454388.1:c.10954G>T	XP_024310156.1:p.Glu3652Ter
XM_024454389.1:c.10543G>T	XP_024310157.1:p.Glu3515Ter