Canonical Allele Identifier: CA1528441073
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13792364_13792366delinsCTT , CM000667.2:g.13792364_13792366delinsCTT GRCh38
NC_000005.9:g.13792473_13792475delinsCTT , CM000667.1:g.13792473_13792475delinsCTT GRCh37
NC_000005.8:g.13845473_13845475delinsCTT NCBI36
NG_013081.1:g.157115_157117delinsAAG
NG_013081.2:g.157115_157117delinsAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.8225-149_8225-147delinsAAG MANE Select ENSP00000265104.4:n.8225-149_8225-147delinsAAG
ENST00000681290.1:c.8180-149_8180-147delinsAAG ENSP00000505288.1:n.8180-149_8180-147delinsAAG
ENST00000265104.4:c.8225-149_8225-147delinsAAG ENSP00000265104.4:n.8225-149_8225-147delinsAAG
NM_001369.2:c.8225-149_8225-147delinsAAG NP_001360.1:n.8225-149_8225-147delinsAAG
XM_005248262.2:c.8180-149_8180-147delinsAAG XP_005248319.1:n.8180-149_8180-147delinsAAG
XM_011513990.1:c.8225-149_8225-147delinsAAG XP_011512292.1:n.8225-149_8225-147delinsAAG
XR_925598.1:n.8432-149_8432-147delinsAAG
XM_005248262.3:c.8333-149_8333-147delinsAAG XP_005248319.2:n.8333-149_8333-147delinsAAG
XM_017009177.1:c.8333-149_8333-147delinsAAG XP_016864666.1:n.8333-149_8333-147delinsAAG
XM_017009178.1:c.7238-149_7238-147delinsAAG XP_016864667.1:n.7238-149_7238-147delinsAAG
XM_017009179.2:c.7238-149_7238-147delinsAAG XP_016864668.1:n.7238-149_7238-147delinsAAG
XM_017009180.1:c.8333-149_8333-147delinsAAG XP_016864669.1:n.8333-149_8333-147delinsAAG
XM_017009181.1:c.8333-149_8333-147delinsAAG XP_016864670.1:n.8333-149_8333-147delinsAAG
XM_017009182.1:c.8333-149_8333-147delinsAAG XP_016864671.1:n.8333-149_8333-147delinsAAG
XM_017009183.1:c.8333-149_8333-147delinsAAG XP_016864672.1:n.8333-149_8333-147delinsAAG
XM_017009184.1:c.8333-149_8333-147delinsAAG XP_016864673.1:n.8333-149_8333-147delinsAAG
XM_017009185.1:c.3422-149_3422-147delinsAAG XP_016864674.1:n.3422-149_3422-147delinsAAG
XM_017009186.1:c.2975-149_2975-147delinsAAG XP_016864675.1:n.2975-149_2975-147delinsAAG
XM_017009188.1:c.2312-149_2312-147delinsAAG XP_016864677.1:n.2312-149_2312-147delinsAAG
XM_024454388.1:c.7238-149_7238-147delinsAAG XP_024310156.1:n.7238-149_7238-147delinsAAG
XM_024454389.1:c.6827-149_6827-147delinsAAG XP_024310157.1:n.6827-149_6827-147delinsAAG
XR_001742034.1:n.8350-149_8350-147delinsAAG
XR_001742035.1:n.8350-149_8350-147delinsAAG
NM_001369.3:c.8225-149_8225-147delinsAAG MANE Select NP_001360.1:n.8225-149_8225-147delinsAAG