Canonical Allele Identifier: CA1528431246
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13770949_13770953delinsAATAT , CM000667.2:g.13770949_13770953delinsAATAT GRCh38
NC_000005.9:g.13771058_13771062delinsAATAT , CM000667.1:g.13771058_13771062delinsAATAT GRCh37
NC_000005.8:g.13824058_13824062delinsAATAT NCBI36
NG_013081.1:g.178528_178532delinsATATT
NG_013081.2:g.178528_178532delinsATATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.9401_9405delinsATATT MANE Select ENSP00000265104.4:p.Asp3134=
ENST00000681290.1:c.9356_9360delinsATATT ENSP00000505288.1:p.Asp3119=
ENST00000265104.4:c.9401_9405delinsATATT ENSP00000265104.4:p.Asp3134=
ENST00000504001.3:n.113_117delinsATATT
NM_001369.2:c.9401_9405delinsATATT NP_001360.1:p.Asp3134=
XM_005248262.2:c.9356_9360delinsATATT XP_005248319.1:p.Asp3119=
XM_005248262.3:c.9509_9513delinsATATT XP_005248319.2:p.Asp3170=
XM_017009177.1:c.9509_9513delinsATATT XP_016864666.1:p.Asp3170=
XM_017009178.1:c.8414_8418delinsATATT XP_016864667.1:p.Asp2805=
XM_017009179.2:c.8414_8418delinsATATT XP_016864668.1:p.Asp2805=
XM_017009180.1:c.9509_9513delinsATATT XP_016864669.1:p.Asp3170=
XM_017009181.1:c.9509_9513delinsATATT XP_016864670.1:p.Asp3170=
XM_017009182.1:c.9509_9513delinsATATT XP_016864671.1:p.Asp3170=
XM_017009183.1:c.9509_9513delinsATATT XP_016864672.1:p.Asp3170=
XM_017009185.1:c.4598_4602delinsATATT XP_016864674.1:p.Asp1533=
XM_017009186.1:c.4151_4155delinsATATT XP_016864675.1:p.Asp1384=
XM_017009188.1:c.3488_3492delinsATATT XP_016864677.1:p.Asp1163=
XM_024454388.1:c.8414_8418delinsATATT XP_024310156.1:p.Asp2805=
XM_024454389.1:c.8003_8007delinsATATT XP_024310157.1:p.Asp2668=
NM_001369.3:c.9401_9405delinsATATT MANE Select NP_001360.1:p.Asp3134=