Canonical Allele Identifier: CA16611868

Gene: DNAH5

Linked Data

• ClinVar Variation Id: 407212
• ClinVar RCV Id: RCV000457343
• dbSNP Id: rs1060501455
• MyVariant Identifiers: chr5:g.13789007C>T (hg19) ; chr5:g.13788898C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13788898C>T , CM000667.2:g.13788898C>T	GRCh38
NC_000005.9:g.13789007C>T , CM000667.1:g.13789007C>T	GRCh37
NC_000005.8:g.13842007C>T	NCBI36
NG_013081.1:g.160583G>A
NG_013081.2:g.160583G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8465G>A MANE Select	ENSP00000265104.4:p.Trp2822Ter
ENST00000681290.1:c.8420G>A	ENSP00000505288.1:p.Trp2807Ter
ENST00000265104.4:c.8465G>A	ENSP00000265104.4:p.Trp2822Ter
NM_001369.2:c.8465G>A	NP_001360.1:p.Trp2822Ter
XM_005248262.2:c.8420G>A	XP_005248319.1:p.Trp2807Ter
XM_011513990.1:c.8465G>A	XP_011512292.1:p.Trp2822Ter
XR_925598.1:n.8672G>A
XM_005248262.3:c.8573G>A	XP_005248319.2:p.Trp2858Ter
XM_017009177.1:c.8573G>A	XP_016864666.1:p.Trp2858Ter
XM_017009178.1:c.7478G>A	XP_016864667.1:p.Trp2493Ter
XM_017009179.2:c.7478G>A	XP_016864668.1:p.Trp2493Ter
XM_017009180.1:c.8573G>A	XP_016864669.1:p.Trp2858Ter
XM_017009181.1:c.8573G>A	XP_016864670.1:p.Trp2858Ter
XM_017009182.1:c.8573G>A	XP_016864671.1:p.Trp2858Ter
XM_017009183.1:c.8573G>A	XP_016864672.1:p.Trp2858Ter
XM_017009184.1:c.8573G>A	XP_016864673.1:p.Trp2858Ter
XM_017009185.1:c.3662G>A	XP_016864674.1:p.Trp1221Ter
XM_017009186.1:c.3215G>A	XP_016864675.1:p.Trp1072Ter
XM_017009188.1:c.2552G>A	XP_016864677.1:p.Trp851Ter
XM_024454388.1:c.7478G>A	XP_024310156.1:p.Trp2493Ter
XM_024454389.1:c.7067G>A	XP_024310157.1:p.Trp2356Ter
XR_001742034.1:n.8590G>A
XR_001742035.1:n.8590G>A
NM_001369.3:c.8465G>A MANE Select	NP_001360.1:p.Trp2822Ter