Canonical Allele Identifier: CA1528415119

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13735873T= , CM000667.2:g.13735873T=	GRCh38
NC_000005.9:g.13735982T= , CM000667.1:g.13735982T=	GRCh37
NC_000005.8:g.13788982T=	NCBI36
NG_013081.1:g.213608A=
NG_013081.2:g.213608A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.11515A= MANE Select	ENSP00000265104.4:p.Met3839=
ENST00000681290.1:c.11470A=	ENSP00000505288.1:p.Met3824=
ENST00000265104.4:c.11515A=	ENSP00000265104.4:p.Met3839=
NM_001369.2:c.11515A=	NP_001360.1:p.Met3839=
XM_005248262.2:c.11470A=	XP_005248319.1:p.Met3824=
XM_005248262.3:c.11623A=	XP_005248319.2:p.Met3875=
XM_017009177.1:c.11623A=	XP_016864666.1:p.Met3875=
XM_017009178.1:c.10528A=	XP_016864667.1:p.Met3510=
XM_017009179.2:c.10528A=	XP_016864668.1:p.Met3510=
XM_017009180.1:c.11623A=	XP_016864669.1:p.Met3875=
XM_017009181.1:c.11623A=	XP_016864670.1:p.Met3875=
XM_017009182.1:c.11379A=	XP_016864671.1:p.Arg3793=
XM_017009185.1:c.6712A=	XP_016864674.1:p.Met2238=
XM_017009186.1:c.6265A=	XP_016864675.1:p.Met2089=
XM_017009188.1:c.5602A=	XP_016864677.1:p.Met1868=
XM_024454388.1:c.10528A=	XP_024310156.1:p.Met3510=
XM_024454389.1:c.10117A=	XP_024310157.1:p.Met3373=
NM_001369.3:c.11515A= MANE Select	NP_001360.1:p.Met3839=