Canonical Allele Identifier: CA1528395903
Gene: DNAH5 HGNC NCBI

Linked Data

dbSNP Id: rs1740777780

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13692149A>T , CM000667.2:g.13692149A>T GRCh38
NC_000005.9:g.13692258A>T , CM000667.1:g.13692258A>T GRCh37
NC_000005.8:g.13745258A>T NCBI36
NG_013081.1:g.257332T>A
NG_013081.2:g.257332T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000683611.1:n.1057-14T>A
ENST00000265104.5:c.13724-14T>A MANE Select ENSP00000265104.4:n.13724-14T>A
ENST00000681290.1:c.13679-14T>A ENSP00000505288.1:n.13679-14T>A
ENST00000265104.4:c.13724-14T>A ENSP00000265104.4:n.13724-14T>A
NM_001369.2:c.13724-14T>A NP_001360.1:n.13724-14T>A
XM_005248262.2:c.13679-14T>A XP_005248319.1:n.13679-14T>A
XM_005248262.3:c.13832-14T>A XP_005248319.2:n.13832-14T>A
XM_017009177.1:c.13412-14T>A XP_016864666.1:n.13412-14T>A
XM_017009178.1:c.12737-14T>A XP_016864667.1:n.12737-14T>A
XM_017009179.2:c.12737-14T>A XP_016864668.1:n.12737-14T>A
XM_017009185.1:c.8921-14T>A XP_016864674.1:n.8921-14T>A
XM_017009186.1:c.8474-14T>A XP_016864675.1:n.8474-14T>A
XM_017009188.1:c.7811-14T>A XP_016864677.1:n.7811-14T>A
XM_024454388.1:c.12737-14T>A XP_024310156.1:n.12737-14T>A
XM_024454389.1:c.12326-14T>A XP_024310157.1:n.12326-14T>A
NM_001369.3:c.13724-14T>A MANE Select NP_001360.1:n.13724-14T>A