Canonical Allele Identifier: CA1528415158
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13735965_13735972delinsCGAGAGAG , CM000667.2:g.13735965_13735972delinsCGAGAGAG GRCh38
NC_000005.9:g.13736074_13736081delinsCGAGAGAG , CM000667.1:g.13736074_13736081delinsCGAGAGAG GRCh37
NC_000005.8:g.13789074_13789081delinsCGAGAGAG NCBI36
NG_013081.1:g.213509_213516delinsCTCTCTCG
NG_013081.2:g.213509_213516delinsCTCTCTCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.11456-40_11456-33delinsCTCTCTCG MANE Select ENSP00000265104.4:n.11456-40_11456-33delinsCTCTCTCG
ENST00000681290.1:c.11411-40_11411-33delinsCTCTCTCG ENSP00000505288.1:n.11411-40_11411-33delinsCTCTCTCG
ENST00000265104.4:c.11456-40_11456-33delinsCTCTCTCG ENSP00000265104.4:n.11456-40_11456-33delinsCTCTCTCG
NM_001369.2:c.11456-40_11456-33delinsCTCTCTCG NP_001360.1:n.11456-40_11456-33delinsCTCTCTCG
XM_005248262.2:c.11411-40_11411-33delinsCTCTCTCG XP_005248319.1:n.11411-40_11411-33delinsCTCTCTCG
XM_005248262.3:c.11564-40_11564-33delinsCTCTCTCG XP_005248319.2:n.11564-40_11564-33delinsCTCTCTCG
XM_017009177.1:c.11564-40_11564-33delinsCTCTCTCG XP_016864666.1:n.11564-40_11564-33delinsCTCTCTCG
XM_017009178.1:c.10469-40_10469-33delinsCTCTCTCG XP_016864667.1:n.10469-40_10469-33delinsCTCTCTCG
XM_017009179.2:c.10469-40_10469-33delinsCTCTCTCG XP_016864668.1:n.10469-40_10469-33delinsCTCTCTCG
XM_017009180.1:c.11564-40_11564-33delinsCTCTCTCG XP_016864669.1:n.11564-40_11564-33delinsCTCTCTCG
XM_017009181.1:c.11564-40_11564-33delinsCTCTCTCG XP_016864670.1:n.11564-40_11564-33delinsCTCTCTCG
XM_017009182.1:c.11320-40_11320-33delinsCTCTCTCG XP_016864671.1:n.11320-40_11320-33delinsCTCTCTCG
XM_017009185.1:c.6653-40_6653-33delinsCTCTCTCG XP_016864674.1:n.6653-40_6653-33delinsCTCTCTCG
XM_017009186.1:c.6206-40_6206-33delinsCTCTCTCG XP_016864675.1:n.6206-40_6206-33delinsCTCTCTCG
XM_017009188.1:c.5543-40_5543-33delinsCTCTCTCG XP_016864677.1:n.5543-40_5543-33delinsCTCTCTCG
XM_024454388.1:c.10469-40_10469-33delinsCTCTCTCG XP_024310156.1:n.10469-40_10469-33delinsCTCTCTCG
XM_024454389.1:c.10058-40_10058-33delinsCTCTCTCG XP_024310157.1:n.10058-40_10058-33delinsCTCTCTCG
NM_001369.3:c.11456-40_11456-33delinsCTCTCTCG MANE Select NP_001360.1:n.11456-40_11456-33delinsCTCTCTCG