Canonical Allele Identifier: CA916084225
Gene: DNAH5 HGNC NCBI

Linked Data

ClinVar Variation Id: 869386
ClinVar RCV Id: RCV001078463

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13764772_13769751delinsTAA , CM000667.2:g.13764772_13769751delinsTAA GRCh38
NC_000005.9:g.13764881_13769860delinsTAA , CM000667.1:g.13764881_13769860delinsTAA GRCh37
NC_000005.8:g.13817881_13822860delinsTAA NCBI36
NG_013081.1:g.179730_184709delinsTTA
NG_013081.2:g.179730_184709delinsTTA

Transcript Alleles

HGVS Amino-acid change
ENST00000265104.5:c.9606-136_10101+1204delinsTTA
ENST00000681290.1:c.9561-136_10056+1204delinsTTA
ENST00000265104.4:c.9606-136_10101+1204delinsTTA
ENST00000504001.3:n.318-136_610-1871delinsTTA
NM_001369.2:c.9606-136_10101+1204delinsTTA
XM_005248262.2:c.9561-136_10056+1204delinsTTA
XM_005248262.3:c.9714-136_10209+1204delinsTTA
XM_017009177.1:c.9714-136_10209+1204delinsTTA
XM_017009178.1:c.8619-136_9114+1204delinsTTA
XM_017009179.2:c.8619-136_9114+1204delinsTTA
XM_017009180.1:c.9714-136_10209+1204delinsTTA
XM_017009181.1:c.9714-136_10209+1204delinsTTA
XM_017009182.1:c.9714-136_10209+1204delinsTTA
XM_017009185.1:c.4803-136_5298+1204delinsTTA
XM_017009186.1:c.4356-136_4851+1204delinsTTA
XM_017009188.1:c.3693-136_4188+1204delinsTTA
XM_024454388.1:c.8619-136_9114+1204delinsTTA
XM_024454389.1:c.8208-136_8703+1204delinsTTA
NM_001369.3:c.9606-136_10101+1204delinsTTA