Canonical Allele Identifier: CA443259965
Gene: DNAH5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.13735239del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13735131del , CM000667.2:g.13735131del GRCh38
NC_000005.9:g.13735240del , CM000667.1:g.13735240del GRCh37
NC_000005.8:g.13788240del NCBI36
NG_013081.1:g.214351del
NG_013081.2:g.214351del

Transcript Alleles

HGVS Amino-acid change
ENST00000265104.5:c.11761+1del
ENST00000681290.1:c.11716+1del
ENST00000265104.4:c.11761+1del
NM_001369.2:c.11761+1del
XM_005248262.2:c.11716+1del
XM_005248262.3:c.11869+1del
XM_017009177.1:c.11869+1del
XM_017009178.1:c.10774+1del
XM_017009179.2:c.10774+1del
XM_017009180.1:c.11869+1del
XM_017009181.1:c.11869+1del
XM_017009185.1:c.6958+1del
XM_017009186.1:c.6511+1del
XM_017009188.1:c.5848+1del
XM_024454388.1:c.10774+1del
XM_024454389.1:c.10363+1del
NM_001369.3:c.11761+1del