Canonical Allele Identifier: CA359202036
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13769070T>G , CM000667.2:g.13769070T>G GRCh38
NC_000005.9:g.13769179T>G , CM000667.1:g.13769179T>G GRCh37
NC_000005.8:g.13822179T>G NCBI36
NG_013081.1:g.180411A>C
NG_013081.2:g.180411A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.9787A>C MANE Select ENSP00000265104.4:p.Lys3263Gln
ENST00000681290.1:c.9742A>C ENSP00000505288.1:p.Lys3248Gln
ENST00000265104.4:c.9787A>C ENSP00000265104.4:p.Lys3263Gln
ENST00000504001.3:n.499A>C
NM_001369.2:c.9787A>C NP_001360.1:p.Lys3263Gln
XM_005248262.2:c.9742A>C XP_005248319.1:p.Lys3248Gln
XM_005248262.3:c.9895A>C XP_005248319.2:p.Lys3299Gln
XM_017009177.1:c.9895A>C XP_016864666.1:p.Lys3299Gln
XM_017009178.1:c.8800A>C XP_016864667.1:p.Lys2934Gln
XM_017009179.2:c.8800A>C XP_016864668.1:p.Lys2934Gln
XM_017009180.1:c.9895A>C XP_016864669.1:p.Lys3299Gln
XM_017009181.1:c.9895A>C XP_016864670.1:p.Lys3299Gln
XM_017009182.1:c.9895A>C XP_016864671.1:p.Lys3299Gln
XM_017009185.1:c.4984A>C XP_016864674.1:p.Lys1662Gln
XM_017009186.1:c.4537A>C XP_016864675.1:p.Lys1513Gln
XM_017009188.1:c.3874A>C XP_016864677.1:p.Lys1292Gln
XM_024454388.1:c.8800A>C XP_024310156.1:p.Lys2934Gln
XM_024454389.1:c.8389A>C XP_024310157.1:p.Lys2797Gln
NM_001369.3:c.9787A>C MANE Select NP_001360.1:p.Lys3263Gln