Canonical Allele Identifier: CA359208415

Gene: DNAH5

Linked Data

• ClinVar Variation Id: 1725343
• ClinVar RCV Id: RCV002309027
• MyVariant Identifiers: chr5:g.13776629T>A (hg19) ; chr5:g.13776520T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776520T>A , CM000667.2:g.13776520T>A	GRCh38
NC_000005.9:g.13776629T>A , CM000667.1:g.13776629T>A	GRCh37
NC_000005.8:g.13829629T>A	NCBI36
NG_013081.1:g.172961A>T
NG_013081.2:g.172961A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9292A>T MANE Select	ENSP00000265104.4:p.Arg3098Ter
ENST00000681290.1:c.9247A>T	ENSP00000505288.1:p.Arg3083Ter
ENST00000265104.4:c.9292A>T	ENSP00000265104.4:p.Arg3098Ter
NM_001369.2:c.9292A>T	NP_001360.1:p.Arg3098Ter
XM_005248262.2:c.9247A>T	XP_005248319.1:p.Arg3083Ter
XM_005248262.3:c.9400A>T	XP_005248319.2:p.Arg3134Ter
XM_017009177.1:c.9400A>T	XP_016864666.1:p.Arg3134Ter
XM_017009178.1:c.8305A>T	XP_016864667.1:p.Arg2769Ter
XM_017009179.2:c.8305A>T	XP_016864668.1:p.Arg2769Ter
XM_017009180.1:c.9400A>T	XP_016864669.1:p.Arg3134Ter
XM_017009181.1:c.9400A>T	XP_016864670.1:p.Arg3134Ter
XM_017009182.1:c.9400A>T	XP_016864671.1:p.Arg3134Ter
XM_017009183.1:c.9400A>T	XP_016864672.1:p.Arg3134Ter
XM_017009185.1:c.4489A>T	XP_016864674.1:p.Arg1497Ter
XM_017009186.1:c.4042A>T	XP_016864675.1:p.Arg1348Ter
XM_017009188.1:c.3379A>T	XP_016864677.1:p.Arg1127Ter
XM_024454388.1:c.8305A>T	XP_024310156.1:p.Arg2769Ter
XM_024454389.1:c.7894A>T	XP_024310157.1:p.Arg2632Ter
NM_001369.3:c.9292A>T MANE Select	NP_001360.1:p.Arg3098Ter