Canonical Allele Identifier: CA1528430416
Gene: DNAH5 HGNC NCBI

Linked Data

dbSNP Id: rs1752936643
gnomAD v4: 5-13769172-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13769172C>T , CM000667.2:g.13769172C>T GRCh38
NC_000005.9:g.13769281C>T , CM000667.1:g.13769281C>T GRCh37
NC_000005.8:g.13822281C>T NCBI36
NG_013081.1:g.180309G>A
NG_013081.2:g.180309G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000265104.5:c.9721-36G>A MANE Select ENSP00000265104.4:n.9721-36G>A
ENST00000681290.1:c.9676-36G>A ENSP00000505288.1:n.9676-36G>A
ENST00000265104.4:c.9721-36G>A ENSP00000265104.4:n.9721-36G>A
ENST00000504001.3:n.433-36G>A
NM_001369.2:c.9721-36G>A NP_001360.1:n.9721-36G>A
XM_005248262.2:c.9676-36G>A XP_005248319.1:n.9676-36G>A
XM_005248262.3:c.9829-36G>A XP_005248319.2:n.9829-36G>A
XM_017009177.1:c.9829-36G>A XP_016864666.1:n.9829-36G>A
XM_017009178.1:c.8734-36G>A XP_016864667.1:n.8734-36G>A
XM_017009179.2:c.8734-36G>A XP_016864668.1:n.8734-36G>A
XM_017009180.1:c.9829-36G>A XP_016864669.1:n.9829-36G>A
XM_017009181.1:c.9829-36G>A XP_016864670.1:n.9829-36G>A
XM_017009182.1:c.9829-36G>A XP_016864671.1:n.9829-36G>A
XM_017009185.1:c.4918-36G>A XP_016864674.1:n.4918-36G>A
XM_017009186.1:c.4471-36G>A XP_016864675.1:n.4471-36G>A
XM_017009188.1:c.3808-36G>A XP_016864677.1:n.3808-36G>A
XM_024454388.1:c.8734-36G>A XP_024310156.1:n.8734-36G>A
XM_024454389.1:c.8323-36G>A XP_024310157.1:n.8323-36G>A
NM_001369.3:c.9721-36G>A MANE Select NP_001360.1:n.9721-36G>A