Canonical Allele Identifier: CA364003376
Gene: DNAH8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.38842671A>G , CM000668.2:g.38842671A>G GRCh38
NC_000006.11:g.38810447A>G , CM000668.1:g.38810447A>G GRCh37
NC_000006.10:g.38918425A>G NCBI36
NG_041805.1:g.132331A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000327475.11:c.4613A>G MANE Select ENSP00000333363.7:p.Lys1538Arg
ENST00000327475.10:c.4613A>G ENSP00000333363.7:p.Lys1538Arg
ENST00000359357.7:c.3962A>G ENSP00000352312.3:p.Lys1321Arg
ENST00000449981.6:c.4613A>G ENSP00000415331.2:p.Lys1538Arg
NM_001206927.1:c.4613A>G NP_001193856.1:p.Lys1538Arg
XM_011514318.1:c.4550A>G XP_011512620.1:p.Lys1517Arg
XM_011514319.1:c.4613A>G XP_011512621.1:p.Lys1538Arg
XM_011514320.1:c.4376A>G XP_011512622.1:p.Lys1459Arg
XM_011514321.1:c.3962A>G XP_011512623.1:p.Lys1321Arg
XM_011514322.1:c.4613A>G XP_011512624.1:p.Lys1538Arg
XR_926078.1:n.4730A>G
NM_001371.3:c.3962A>G NP_001362.2:p.Lys1321Arg
XM_011514318.2:c.4550A>G XP_011512620.1:p.Lys1517Arg
XM_011514319.2:c.4613A>G XP_011512621.1:p.Lys1538Arg
XM_011514320.2:c.4376A>G XP_011512622.1:p.Lys1459Arg
XM_017010325.1:c.4613A>G XP_016865814.1:p.Lys1538Arg
XM_017010326.1:c.4613A>G XP_016865815.1:p.Lys1538Arg
XM_017010327.1:c.4613A>G XP_016865816.1:p.Lys1538Arg
XR_001743188.1:n.4734A>G
XR_926078.2:n.4733A>G
NM_001206927.2:c.4613A>G MANE Select NP_001193856.1:p.Lys1538Arg
NM_001371.4:c.3962A>G NP_001362.2:p.Lys1321Arg