Canonical Allele Identifier: CA1528431198

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13770820G= , CM000667.2:g.13770820G=	GRCh38
NC_000005.9:g.13770929G= , CM000667.1:g.13770929G=	GRCh37
NC_000005.8:g.13823929G=	NCBI36
NG_013081.1:g.178661C=
NG_013081.2:g.178661C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9534C= MANE Select	ENSP00000265104.4:p.Tyr3178=
ENST00000681290.1:c.9489C=	ENSP00000505288.1:p.Tyr3163=
ENST00000265104.4:c.9534C=	ENSP00000265104.4:p.Tyr3178=
ENST00000504001.3:n.246C=
NM_001369.2:c.9534C=	NP_001360.1:p.Tyr3178=
XM_005248262.2:c.9489C=	XP_005248319.1:p.Tyr3163=
XM_005248262.3:c.9642C=	XP_005248319.2:p.Tyr3214=
XM_017009177.1:c.9642C=	XP_016864666.1:p.Tyr3214=
XM_017009178.1:c.8547C=	XP_016864667.1:p.Tyr2849=
XM_017009179.2:c.8547C=	XP_016864668.1:p.Tyr2849=
XM_017009180.1:c.9642C=	XP_016864669.1:p.Tyr3214=
XM_017009181.1:c.9642C=	XP_016864670.1:p.Tyr3214=
XM_017009182.1:c.9642C=	XP_016864671.1:p.Tyr3214=
XM_017009183.1:c.9642C=	XP_016864672.1:p.Tyr3214=
XM_017009185.1:c.4731C=	XP_016864674.1:p.Tyr1577=
XM_017009186.1:c.4284C=	XP_016864675.1:p.Tyr1428=
XM_017009188.1:c.3621C=	XP_016864677.1:p.Tyr1207=
XM_024454388.1:c.8547C=	XP_024310156.1:p.Tyr2849=
XM_024454389.1:c.8136C=	XP_024310157.1:p.Tyr2712=
NM_001369.3:c.9534C= MANE Select	NP_001360.1:p.Tyr3178=