Canonical Allele Identifier: CA3203425

Gene: DNAH5

Linked Data

• dbSNP Id: rs777296535
• ExAC: 5:13829698 C / T
• MyVariant Identifiers: chr5:g.13829698C>T (hg19) ; chr5:g.13829589C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13829589C>T , CM000667.2:g.13829589C>T	GRCh38
NC_000005.9:g.13829698C>T , CM000667.1:g.13829698C>T	GRCh37
NC_000005.8:g.13882698C>T	NCBI36
NG_013081.1:g.119892G>A
NG_013081.2:g.119892G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683090.1:n.1296G>A
ENST00000265104.5:c.6365G>A MANE Select	ENSP00000265104.4:p.Cys2122Tyr
ENST00000681290.1:c.6320G>A	ENSP00000505288.1:p.Cys2107Tyr
ENST00000265104.4:c.6365G>A	ENSP00000265104.4:p.Cys2122Tyr
NM_001369.2:c.6365G>A	NP_001360.1:p.Cys2122Tyr
XM_005248262.2:c.6320G>A	XP_005248319.1:p.Cys2107Tyr
XM_011513990.1:c.6365G>A	XP_011512292.1:p.Cys2122Tyr
XR_925598.1:n.6572G>A
XM_005248262.3:c.6473G>A	XP_005248319.2:p.Cys2158Tyr
XM_017009177.1:c.6473G>A	XP_016864666.1:p.Cys2158Tyr
XM_017009178.1:c.5378G>A	XP_016864667.1:p.Cys1793Tyr
XM_017009179.2:c.5378G>A	XP_016864668.1:p.Cys1793Tyr
XM_017009180.1:c.6473G>A	XP_016864669.1:p.Cys2158Tyr
XM_017009181.1:c.6473G>A	XP_016864670.1:p.Cys2158Tyr
XM_017009182.1:c.6473G>A	XP_016864671.1:p.Cys2158Tyr
XM_017009183.1:c.6473G>A	XP_016864672.1:p.Cys2158Tyr
XM_017009184.1:c.6473G>A	XP_016864673.1:p.Cys2158Tyr
XM_017009185.1:c.1562G>A	XP_016864674.1:p.Cys521Tyr
XM_017009186.1:c.1115G>A	XP_016864675.1:p.Cys372Tyr
XM_017009187.1:c.6473G>A	XP_016864676.1:p.Cys2158Tyr
XM_017009188.1:c.452G>A	XP_016864677.1:p.Cys151Tyr
XM_024454388.1:c.5378G>A	XP_024310156.1:p.Cys1793Tyr
XM_024454389.1:c.4967G>A	XP_024310157.1:p.Cys1656Tyr
XR_001742034.1:n.6490G>A
XR_001742035.1:n.6490G>A
NM_001369.3:c.6365G>A MANE Select	NP_001360.1:p.Cys2122Tyr