Canonical Allele Identifier: CA1528423502

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753408A= , CM000667.2:g.13753408A=	GRCh38
NC_000005.9:g.13753517A= , CM000667.1:g.13753517A=	GRCh37
NC_000005.8:g.13806517A=	NCBI36
NG_013081.1:g.196073T=
NG_013081.2:g.196073T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10697T= MANE Select	ENSP00000265104.4:p.Met3566=
ENST00000681290.1:c.10652T=	ENSP00000505288.1:p.Met3551=
ENST00000265104.4:c.10697T=	ENSP00000265104.4:p.Met3566=
NM_001369.2:c.10697T=	NP_001360.1:p.Met3566=
XM_005248262.2:c.10652T=	XP_005248319.1:p.Met3551=
XM_005248262.3:c.10805T=	XP_005248319.2:p.Met3602=
XM_017009177.1:c.10805T=	XP_016864666.1:p.Met3602=
XM_017009178.1:c.9710T=	XP_016864667.1:p.Met3237=
XM_017009179.2:c.9710T=	XP_016864668.1:p.Met3237=
XM_017009180.1:c.10805T=	XP_016864669.1:p.Met3602=
XM_017009181.1:c.10805T=	XP_016864670.1:p.Met3602=
XM_017009182.1:c.10805T=	XP_016864671.1:p.Met3602=
XM_017009185.1:c.5894T=	XP_016864674.1:p.Met1965=
XM_017009186.1:c.5447T=	XP_016864675.1:p.Met1816=
XM_017009188.1:c.4784T=	XP_016864677.1:p.Met1595=
XM_024454388.1:c.9710T=	XP_024310156.1:p.Met3237=
XM_024454389.1:c.9299T=	XP_024310157.1:p.Met3100=
NM_001369.3:c.10697T= MANE Select	NP_001360.1:p.Met3566=