Canonical Allele Identifier: CA443535708
Gene: DNAH5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.13776594G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13776485G>A , CM000667.2:g.13776485G>A GRCh38
NC_000005.9:g.13776594G>A , CM000667.1:g.13776594G>A GRCh37
NC_000005.8:g.13829594G>A NCBI36
NG_013081.1:g.172996C>T
NG_013081.2:g.172996C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.9327C>T MANE Select ENSP00000265104.4:p.Cys3109=
ENST00000681290.1:c.9282C>T ENSP00000505288.1:p.Cys3094=
ENST00000265104.4:c.9327C>T ENSP00000265104.4:p.Cys3109=
NM_001369.2:c.9327C>T NP_001360.1:p.Cys3109=
XM_005248262.2:c.9282C>T XP_005248319.1:p.Cys3094=
XM_005248262.3:c.9435C>T XP_005248319.2:p.Cys3145=
XM_017009177.1:c.9435C>T XP_016864666.1:p.Cys3145=
XM_017009178.1:c.8340C>T XP_016864667.1:p.Cys2780=
XM_017009179.2:c.8340C>T XP_016864668.1:p.Cys2780=
XM_017009180.1:c.9435C>T XP_016864669.1:p.Cys3145=
XM_017009181.1:c.9435C>T XP_016864670.1:p.Cys3145=
XM_017009182.1:c.9435C>T XP_016864671.1:p.Cys3145=
XM_017009183.1:c.9435C>T XP_016864672.1:p.Cys3145=
XM_017009185.1:c.4524C>T XP_016864674.1:p.Cys1508=
XM_017009186.1:c.4077C>T XP_016864675.1:p.Cys1359=
XM_017009188.1:c.3414C>T XP_016864677.1:p.Cys1138=
XM_024454388.1:c.8340C>T XP_024310156.1:p.Cys2780=
XM_024454389.1:c.7929C>T XP_024310157.1:p.Cys2643=
NM_001369.3:c.9327C>T MANE Select NP_001360.1:p.Cys3109=