Canonical Allele Identifier: CA1622423997
Gene: DNAH8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.38842596A= , CM000668.2:g.38842596A= GRCh38
NC_000006.11:g.38810372A= , CM000668.1:g.38810372A= GRCh37
NC_000006.10:g.38918350A= NCBI36
NG_041805.1:g.132256A=

Transcript Alleles

HGVS Amino-acid change
ENST00000327475.11:c.4605-67A= MANE Select ENSP00000333363.7:n.4605-67A=
ENST00000327475.10:c.4605-67A= ENSP00000333363.7:n.4605-67A=
ENST00000359357.7:c.3954-67A= ENSP00000352312.3:n.3954-67A=
ENST00000449981.6:c.4605-67A= ENSP00000415331.2:n.4605-67A=
NM_001206927.1:c.4605-67A= NP_001193856.1:n.4605-67A=
XM_011514318.1:c.4542-67A= XP_011512620.1:n.4542-67A=
XM_011514319.1:c.4605-67A= XP_011512621.1:n.4605-67A=
XM_011514320.1:c.4368-67A= XP_011512622.1:n.4368-67A=
XM_011514321.1:c.3954-67A= XP_011512623.1:n.3954-67A=
XM_011514322.1:c.4605-67A= XP_011512624.1:n.4605-67A=
XR_926078.1:n.4722-67A=
NM_001371.3:c.3954-67A= NP_001362.2:n.3954-67A=
XM_011514318.2:c.4542-67A= XP_011512620.1:n.4542-67A=
XM_011514319.2:c.4605-67A= XP_011512621.1:n.4605-67A=
XM_011514320.2:c.4368-67A= XP_011512622.1:n.4368-67A=
XM_017010325.1:c.4605-67A= XP_016865814.1:n.4605-67A=
XM_017010326.1:c.4605-67A= XP_016865815.1:n.4605-67A=
XM_017010327.1:c.4605-67A= XP_016865816.1:n.4605-67A=
XR_001743188.1:n.4726-67A=
XR_926078.2:n.4725-67A=
NM_001206927.2:c.4605-67A= MANE Select NP_001193856.1:n.4605-67A=
NM_001371.4:c.3954-67A= NP_001362.2:n.3954-67A=