Canonical Allele Identifier: CA3790885
Community Standard Title: NM_001206927.2(DNAH8):c.10963-1G>A
Gene: DNAH8 HGNC NCBI
DNAH8-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.38926054G>A , CM000668.2:g.38926054G>A GRCh38
NC_000006.11:g.38893830G>A , CM000668.1:g.38893830G>A GRCh37
NC_000006.10:g.39001808G>A NCBI36
NG_041805.1:g.215714G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001206927.2:c.10963-1G>A (DNAH8) MANE Select NP_001193856.1:n.10963-1G>A
ENST00000327475.11:c.10963-1G>A (DNAH8) MANE Select ENSP00000333363.7:n.10963-1G>A
NM_001206927.1:c.10963-1G>A (DNAH8) NP_001193856.1:n.10963-1G>A
NM_001371.3:c.10312-1G>A (DNAH8) NP_001362.2:n.10312-1G>A
NM_001371.4:c.10312-1G>A (DNAH8) NP_001362.2:n.10312-1G>A
NR_038401.1:n.161-1003C>T (DNAH8-AS1)
ENST00000327475.10:c.10963-1G>A (DNAH8) ENSP00000333363.7:n.10963-1G>A
ENST00000359357.7:c.10312-1G>A (DNAH8) ENSP00000352312.3:n.10312-1G>A
ENST00000449981.6:c.10963-1G>A (DNAH8) ENSP00000415331.2:n.10963-1G>A
XM_011514318.1:c.10900-1G>A (DNAH8) XP_011512620.1:n.10900-1G>A
XM_011514318.2:c.10900-1G>A (DNAH8) XP_011512620.1:n.10900-1G>A
XM_011514319.1:c.10855-1G>A (DNAH8) XP_011512621.1:n.10855-1G>A
XM_011514319.2:c.10855-1G>A (DNAH8) XP_011512621.1:n.10855-1G>A
XM_011514320.1:c.10726-1G>A (DNAH8) XP_011512622.1:n.10726-1G>A
XM_011514320.2:c.10726-1G>A (DNAH8) XP_011512622.1:n.10726-1G>A
XM_011514321.1:c.10312-1G>A (DNAH8) XP_011512623.1:n.10312-1G>A
XM_017010325.1:c.10963-1G>A (DNAH8) XP_016865814.1:n.10963-1G>A
XM_017010326.1:c.10963-1G>A (DNAH8) XP_016865815.1:n.10963-1G>A
XR_926078.1:n.11080-1G>A (DNAH8)
XR_926078.2:n.11083-1G>A (DNAH8)