Canonical Allele Identifier: CA1528430337

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13768987A= , CM000667.2:g.13768987A=	GRCh38
NC_000005.9:g.13769096A= , CM000667.1:g.13769096A=	GRCh37
NC_000005.8:g.13822096A=	NCBI36
NG_013081.1:g.180494T=
NG_013081.2:g.180494T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9870T= MANE Select	ENSP00000265104.4:p.Ala3290=
ENST00000681290.1:c.9825T=	ENSP00000505288.1:p.Ala3275=
ENST00000265104.4:c.9870T=	ENSP00000265104.4:p.Ala3290=
ENST00000504001.3:n.582T=
NM_001369.2:c.9870T=	NP_001360.1:p.Ala3290=
XM_005248262.2:c.9825T=	XP_005248319.1:p.Ala3275=
XM_005248262.3:c.9978T=	XP_005248319.2:p.Ala3326=
XM_017009177.1:c.9978T=	XP_016864666.1:p.Ala3326=
XM_017009178.1:c.8883T=	XP_016864667.1:p.Ala2961=
XM_017009179.2:c.8883T=	XP_016864668.1:p.Ala2961=
XM_017009180.1:c.9978T=	XP_016864669.1:p.Ala3326=
XM_017009181.1:c.9978T=	XP_016864670.1:p.Ala3326=
XM_017009182.1:c.9978T=	XP_016864671.1:p.Ala3326=
XM_017009185.1:c.5067T=	XP_016864674.1:p.Ala1689=
XM_017009186.1:c.4620T=	XP_016864675.1:p.Ala1540=
XM_017009188.1:c.3957T=	XP_016864677.1:p.Ala1319=
XM_024454388.1:c.8883T=	XP_024310156.1:p.Ala2961=
XM_024454389.1:c.8472T=	XP_024310157.1:p.Ala2824=
NM_001369.3:c.9870T= MANE Select	NP_001360.1:p.Ala3290=