Canonical Allele Identifier: CA359208408

Gene: DNAH5

Linked Data

• COSMIC: COSM3608991
• MyVariant Identifiers: chr5:g.13776628C>T (hg19) ; chr5:g.13776519C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776519C>T , CM000667.2:g.13776519C>T	GRCh38
NC_000005.9:g.13776628C>T , CM000667.1:g.13776628C>T	GRCh37
NC_000005.8:g.13829628C>T	NCBI36
NG_013081.1:g.172962G>A
NG_013081.2:g.172962G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9293G>A MANE Select	ENSP00000265104.4:p.Arg3098Lys
ENST00000681290.1:c.9248G>A	ENSP00000505288.1:p.Arg3083Lys
ENST00000265104.4:c.9293G>A	ENSP00000265104.4:p.Arg3098Lys
NM_001369.2:c.9293G>A	NP_001360.1:p.Arg3098Lys
XM_005248262.2:c.9248G>A	XP_005248319.1:p.Arg3083Lys
XM_005248262.3:c.9401G>A	XP_005248319.2:p.Arg3134Lys
XM_017009177.1:c.9401G>A	XP_016864666.1:p.Arg3134Lys
XM_017009178.1:c.8306G>A	XP_016864667.1:p.Arg2769Lys
XM_017009179.2:c.8306G>A	XP_016864668.1:p.Arg2769Lys
XM_017009180.1:c.9401G>A	XP_016864669.1:p.Arg3134Lys
XM_017009181.1:c.9401G>A	XP_016864670.1:p.Arg3134Lys
XM_017009182.1:c.9401G>A	XP_016864671.1:p.Arg3134Lys
XM_017009183.1:c.9401G>A	XP_016864672.1:p.Arg3134Lys
XM_017009185.1:c.4490G>A	XP_016864674.1:p.Arg1497Lys
XM_017009186.1:c.4043G>A	XP_016864675.1:p.Arg1348Lys
XM_017009188.1:c.3380G>A	XP_016864677.1:p.Arg1127Lys
XM_024454388.1:c.8306G>A	XP_024310156.1:p.Arg2769Lys
XM_024454389.1:c.7895G>A	XP_024310157.1:p.Arg2632Lys
NM_001369.3:c.9293G>A MANE Select	NP_001360.1:p.Arg3098Lys