Canonical Allele Identifier: CA359190422
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13752257G>T , CM000667.2:g.13752257G>T GRCh38
NC_000005.9:g.13752366G>T , CM000667.1:g.13752366G>T GRCh37
NC_000005.8:g.13805366G>T NCBI36
NG_013081.1:g.197224C>A
NG_013081.2:g.197224C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000265104.5:c.10905C>A MANE Select ENSP00000265104.4:p.Asn3635Lys
ENST00000681290.1:c.10860C>A ENSP00000505288.1:p.Asn3620Lys
ENST00000265104.4:c.10905C>A ENSP00000265104.4:p.Asn3635Lys
NM_001369.2:c.10905C>A NP_001360.1:p.Asn3635Lys
XM_005248262.2:c.10860C>A XP_005248319.1:p.Asn3620Lys
XM_005248262.3:c.11013C>A XP_005248319.2:p.Asn3671Lys
XM_017009177.1:c.11013C>A XP_016864666.1:p.Asn3671Lys
XM_017009178.1:c.9918C>A XP_016864667.1:p.Asn3306Lys
XM_017009179.2:c.9918C>A XP_016864668.1:p.Asn3306Lys
XM_017009180.1:c.11013C>A XP_016864669.1:p.Asn3671Lys
XM_017009181.1:c.11013C>A XP_016864670.1:p.Asn3671Lys
XM_017009182.1:c.11013C>A XP_016864671.1:p.Asn3671Lys
XM_017009185.1:c.6102C>A XP_016864674.1:p.Asn2034Lys
XM_017009186.1:c.5655C>A XP_016864675.1:p.Asn1885Lys
XM_017009188.1:c.4992C>A XP_016864677.1:p.Asn1664Lys
XM_024454388.1:c.9918C>A XP_024310156.1:p.Asn3306Lys
XM_024454389.1:c.9507C>A XP_024310157.1:p.Asn3169Lys
NM_001369.3:c.10905C>A MANE Select NP_001360.1:p.Asn3635Lys