Canonical Allele Identifier: CA359192042
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13753462T>G , CM000667.2:g.13753462T>G GRCh38
NC_000005.9:g.13753571T>G , CM000667.1:g.13753571T>G GRCh37
NC_000005.8:g.13806571T>G NCBI36
NG_013081.1:g.196019A>C
NG_013081.2:g.196019A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.10643A>C MANE Select ENSP00000265104.4:p.Lys3548Thr
ENST00000681290.1:c.10598A>C ENSP00000505288.1:p.Lys3533Thr
ENST00000265104.4:c.10643A>C ENSP00000265104.4:p.Lys3548Thr
NM_001369.2:c.10643A>C NP_001360.1:p.Lys3548Thr
XM_005248262.2:c.10598A>C XP_005248319.1:p.Lys3533Thr
XM_005248262.3:c.10751A>C XP_005248319.2:p.Lys3584Thr
XM_017009177.1:c.10751A>C XP_016864666.1:p.Lys3584Thr
XM_017009178.1:c.9656A>C XP_016864667.1:p.Lys3219Thr
XM_017009179.2:c.9656A>C XP_016864668.1:p.Lys3219Thr
XM_017009180.1:c.10751A>C XP_016864669.1:p.Lys3584Thr
XM_017009181.1:c.10751A>C XP_016864670.1:p.Lys3584Thr
XM_017009182.1:c.10751A>C XP_016864671.1:p.Lys3584Thr
XM_017009185.1:c.5840A>C XP_016864674.1:p.Lys1947Thr
XM_017009186.1:c.5393A>C XP_016864675.1:p.Lys1798Thr
XM_017009188.1:c.4730A>C XP_016864677.1:p.Lys1577Thr
XM_024454388.1:c.9656A>C XP_024310156.1:p.Lys3219Thr
XM_024454389.1:c.9245A>C XP_024310157.1:p.Lys3082Thr
NM_001369.3:c.10643A>C MANE Select NP_001360.1:p.Lys3548Thr