Canonical Allele Identifier: CA1528435438
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13776694_13776699delinsATAGGT , CM000667.2:g.13776694_13776699delinsATAGGT GRCh38
NC_000005.9:g.13776803_13776808delinsATAGGT , CM000667.1:g.13776803_13776808delinsATAGGT GRCh37
NC_000005.8:g.13829803_13829808delinsATAGGT NCBI36
NG_013081.1:g.172782_172787delinsACCTAT
NG_013081.2:g.172782_172787delinsACCTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.9113_9118delinsACCTAT MANE Select ENSP00000265104.4:p.Asn3038=
ENST00000681290.1:c.9068_9073delinsACCTAT ENSP00000505288.1:p.Asn3023=
ENST00000265104.4:c.9113_9118delinsACCTAT ENSP00000265104.4:p.Asn3038=
NM_001369.2:c.9113_9118delinsACCTAT NP_001360.1:p.Asn3038=
XM_005248262.2:c.9068_9073delinsACCTAT XP_005248319.1:p.Asn3023=
XM_011513990.1:c.9108_*5delinsACCTAT XP_011512292.1:n.[c.9108_*5delinsACCTAT;Ter3036=]
XR_925598.1:n.9184_9189delinsACCTAT
XM_005248262.3:c.9221_9226delinsACCTAT XP_005248319.2:p.Asn3074=
XM_017009177.1:c.9221_9226delinsACCTAT XP_016864666.1:p.Asn3074=
XM_017009178.1:c.8126_8131delinsACCTAT XP_016864667.1:p.Asn2709=
XM_017009179.2:c.8126_8131delinsACCTAT XP_016864668.1:p.Asn2709=
XM_017009180.1:c.9221_9226delinsACCTAT XP_016864669.1:p.Asn3074=
XM_017009181.1:c.9221_9226delinsACCTAT XP_016864670.1:p.Asn3074=
XM_017009182.1:c.9221_9226delinsACCTAT XP_016864671.1:p.Asn3074=
XM_017009183.1:c.9221_9226delinsACCTAT XP_016864672.1:p.Asn3074=
XM_017009184.1:c.9216_*5delinsACCTAT XP_016864673.1:n.[c.9216_*5delinsACCTAT;Ter3072=]
XM_017009185.1:c.4310_4315delinsACCTAT XP_016864674.1:p.Asn1437=
XM_017009186.1:c.3863_3868delinsACCTAT XP_016864675.1:p.Asn1288=
XM_017009188.1:c.3200_3205delinsACCTAT XP_016864677.1:p.Asn1067=
XM_024454388.1:c.8126_8131delinsACCTAT XP_024310156.1:p.Asn2709=
XM_024454389.1:c.7715_7720delinsACCTAT XP_024310157.1:p.Asn2572=
XR_001742034.1:n.9107_9112delinsACCTAT
XR_001742035.1:n.9102_9107delinsACCTAT
NM_001369.3:c.9113_9118delinsACCTAT MANE Select NP_001360.1:p.Asn3038=