Canonical Allele Identifier: CA3789175

Gene: DNAH8

Linked Data

• dbSNP Id: rs749996981
• ExAC: 6:38810412 TA / T
• gnomAD v2: 6-38810412-TA-T
• gnomAD v3: 6-38842636-TA-T
• gnomAD v4: 6-38842636-TA-T
• MyVariant Identifiers: chr6:g.38810413del (hg19) ; chr6:g.38842637del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.38842637del , CM000668.2:g.38842637del	GRCh38
NC_000006.11:g.38810413del , CM000668.1:g.38810413del	GRCh37
NC_000006.10:g.38918391del	NCBI36
NG_041805.1:g.132297del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327475.11:c.4605-26del MANE Select	ENSP00000333363.7:n.4605-26del
ENST00000327475.10:c.4605-26del	ENSP00000333363.7:n.4605-26del
ENST00000359357.7:c.3954-26del	ENSP00000352312.3:n.3954-26del
ENST00000449981.6:c.4605-26del	ENSP00000415331.2:n.4605-26del
NM_001206927.1:c.4605-26del	NP_001193856.1:n.4605-26del
XM_011514318.1:c.4542-26del	XP_011512620.1:n.4542-26del
XM_011514319.1:c.4605-26del	XP_011512621.1:n.4605-26del
XM_011514320.1:c.4368-26del	XP_011512622.1:n.4368-26del
XM_011514321.1:c.3954-26del	XP_011512623.1:n.3954-26del
XM_011514322.1:c.4605-26del	XP_011512624.1:n.4605-26del
XR_926078.1:n.4722-26del
NM_001371.3:c.3954-26del	NP_001362.2:n.3954-26del
XM_011514318.2:c.4542-26del	XP_011512620.1:n.4542-26del
XM_011514319.2:c.4605-26del	XP_011512621.1:n.4605-26del
XM_011514320.2:c.4368-26del	XP_011512622.1:n.4368-26del
XM_017010325.1:c.4605-26del	XP_016865814.1:n.4605-26del
XM_017010326.1:c.4605-26del	XP_016865815.1:n.4605-26del
XM_017010327.1:c.4605-26del	XP_016865816.1:n.4605-26del
XR_001743188.1:n.4726-26del
XR_926078.2:n.4725-26del
NM_001206927.2:c.4605-26del MANE Select	NP_001193856.1:n.4605-26del
NM_001371.4:c.3954-26del	NP_001362.2:n.3954-26del