Canonical Allele Identifier: CA3790774

Gene: DNAH8 DNAH8-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.38921481T>C , CM000668.2:g.38921481T>C	GRCh38
NC_000006.11:g.38889257T>C , CM000668.1:g.38889257T>C	GRCh37
NC_000006.10:g.38997235T>C	NCBI36
NG_041805.1:g.211141T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001206927.2:c.10637T>C (DNAH8) MANE Select	NP_001193856.1:p.Phe3546Ser
ENST00000327475.11:c.10637T>C (DNAH8) MANE Select	ENSP00000333363.7:p.Phe3546Ser
NM_001206927.1:c.10637T>C (DNAH8)	NP_001193856.1:p.Phe3546Ser
NM_001371.3:c.9986T>C (DNAH8)	NP_001362.2:p.Phe3329Ser
NM_001371.4:c.9986T>C (DNAH8)	NP_001362.2:p.Phe3329Ser
NR_038401.1:n.782+1604A>G (DNAH8-AS1)
ENST00000327475.10:c.10637T>C (DNAH8)	ENSP00000333363.7:p.Phe3546Ser
ENST00000359357.7:c.9986T>C (DNAH8)	ENSP00000352312.3:p.Phe3329Ser
ENST00000449981.6:c.10637T>C (DNAH8)	ENSP00000415331.2:p.Phe3546Ser
XM_011514318.1:c.10574T>C (DNAH8)	XP_011512620.1:p.Phe3525Ser
XM_011514318.2:c.10574T>C (DNAH8)	XP_011512620.1:p.Phe3525Ser
XM_011514319.1:c.10529T>C (DNAH8)	XP_011512621.1:p.Phe3510Ser
XM_011514319.2:c.10529T>C (DNAH8)	XP_011512621.1:p.Phe3510Ser
XM_011514320.1:c.10400T>C (DNAH8)	XP_011512622.1:p.Phe3467Ser
XM_011514320.2:c.10400T>C (DNAH8)	XP_011512622.1:p.Phe3467Ser
XM_011514321.1:c.9986T>C (DNAH8)	XP_011512623.1:p.Phe3329Ser
XM_017010325.1:c.10637T>C (DNAH8)	XP_016865814.1:p.Phe3546Ser
XM_017010326.1:c.10637T>C (DNAH8)	XP_016865815.1:p.Phe3546Ser
XR_926078.1:n.10754T>C (DNAH8)
XR_926078.2:n.10757T>C (DNAH8)