Canonical Allele Identifier: CA1528430368
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13769055C= , CM000667.2:g.13769055C= GRCh38
NC_000005.9:g.13769164C= , CM000667.1:g.13769164C= GRCh37
NC_000005.8:g.13822164C= NCBI36
NG_013081.1:g.180426G=
NG_013081.2:g.180426G=

Transcript Alleles

HGVS Amino-acid change
ENST00000265104.5:c.9802G= MANE Select ENSP00000265104.4:p.Ala3268=
ENST00000681290.1:c.9757G= ENSP00000505288.1:p.Ala3253=
ENST00000265104.4:c.9802G= ENSP00000265104.4:p.Ala3268=
ENST00000504001.3:n.514G=
NM_001369.2:c.9802G= NP_001360.1:p.Ala3268=
XM_005248262.2:c.9757G= XP_005248319.1:p.Ala3253=
XM_005248262.3:c.9910G= XP_005248319.2:p.Ala3304=
XM_017009177.1:c.9910G= XP_016864666.1:p.Ala3304=
XM_017009178.1:c.8815G= XP_016864667.1:p.Ala2939=
XM_017009179.2:c.8815G= XP_016864668.1:p.Ala2939=
XM_017009180.1:c.9910G= XP_016864669.1:p.Ala3304=
XM_017009181.1:c.9910G= XP_016864670.1:p.Ala3304=
XM_017009182.1:c.9910G= XP_016864671.1:p.Ala3304=
XM_017009185.1:c.4999G= XP_016864674.1:p.Ala1667=
XM_017009186.1:c.4552G= XP_016864675.1:p.Ala1518=
XM_017009188.1:c.3889G= XP_016864677.1:p.Ala1297=
XM_024454388.1:c.8815G= XP_024310156.1:p.Ala2939=
XM_024454389.1:c.8404G= XP_024310157.1:p.Ala2802=
NM_001369.3:c.9802G= MANE Select NP_001360.1:p.Ala3268=