Canonical Allele Identifier: CA1528423676
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13753815_13753821delinsCTAAGTT , CM000667.2:g.13753815_13753821delinsCTAAGTT GRCh38
NC_000005.9:g.13753924_13753930delinsCTAAGTT , CM000667.1:g.13753924_13753930delinsCTAAGTT GRCh37
NC_000005.8:g.13806924_13806930delinsCTAAGTT NCBI36
NG_013081.1:g.195660_195666delinsAACTTAG
NG_013081.2:g.195660_195666delinsAACTTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.10556-272_10556-266delinsAACTTAG MANE Select ENSP00000265104.4:n.10556-272_10556-266delinsAACTTAG
ENST00000681290.1:c.10511-272_10511-266delinsAACTTAG ENSP00000505288.1:n.10511-272_10511-266delinsAACTTAG
ENST00000265104.4:c.10556-272_10556-266delinsAACTTAG ENSP00000265104.4:n.10556-272_10556-266delinsAACTTAG
NM_001369.2:c.10556-272_10556-266delinsAACTTAG NP_001360.1:n.10556-272_10556-266delinsAACTTAG
XM_005248262.2:c.10511-272_10511-266delinsAACTTAG XP_005248319.1:n.10511-272_10511-266delinsAACTTAG
XM_005248262.3:c.10664-272_10664-266delinsAACTTAG XP_005248319.2:n.10664-272_10664-266delinsAACTTAG
XM_017009177.1:c.10664-272_10664-266delinsAACTTAG XP_016864666.1:n.10664-272_10664-266delinsAACTTAG
XM_017009178.1:c.9569-272_9569-266delinsAACTTAG XP_016864667.1:n.9569-272_9569-266delinsAACTTAG
XM_017009179.2:c.9569-272_9569-266delinsAACTTAG XP_016864668.1:n.9569-272_9569-266delinsAACTTAG
XM_017009180.1:c.10664-272_10664-266delinsAACTTAG XP_016864669.1:n.10664-272_10664-266delinsAACTTAG
XM_017009181.1:c.10664-272_10664-266delinsAACTTAG XP_016864670.1:n.10664-272_10664-266delinsAACTTAG
XM_017009182.1:c.10664-272_10664-266delinsAACTTAG XP_016864671.1:n.10664-272_10664-266delinsAACTTAG
XM_017009185.1:c.5753-272_5753-266delinsAACTTAG XP_016864674.1:n.5753-272_5753-266delinsAACTTAG
XM_017009186.1:c.5306-272_5306-266delinsAACTTAG XP_016864675.1:n.5306-272_5306-266delinsAACTTAG
XM_017009188.1:c.4643-272_4643-266delinsAACTTAG XP_016864677.1:n.4643-272_4643-266delinsAACTTAG
XM_024454388.1:c.9569-272_9569-266delinsAACTTAG XP_024310156.1:n.9569-272_9569-266delinsAACTTAG
XM_024454389.1:c.9158-272_9158-266delinsAACTTAG XP_024310157.1:n.9158-272_9158-266delinsAACTTAG
NM_001369.3:c.10556-272_10556-266delinsAACTTAG MANE Select NP_001360.1:n.10556-272_10556-266delinsAACTTAG