Canonical Allele Identifier: CA566705634

Gene: DNAH8

Linked Data

• dbSNP Id: rs1360257113
• gnomAD v2: 6-38810368-G-GTTTTA
• gnomAD v3: 6-38842592-G-GTTTTA
• gnomAD v4: 6-38842592-G-GTTTTA
• MyVariant Identifiers: chr6:g.38810368_38810369insTTTTA (hg19) ; chr6:g.38842592_38842593insTTTTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.38842593_38842594insTTTAT , CM000668.2:g.38842593_38842594insTTTAT	GRCh38
NC_000006.11:g.38810369_38810370insTTTAT , CM000668.1:g.38810369_38810370insTTTAT	GRCh37
NC_000006.10:g.38918347_38918348insTTTAT	NCBI36
NG_041805.1:g.132253_132254insTTTAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000327475.11:c.4605-70_4605-69insTTTAT MANE Select	ENSP00000333363.7:n.4605-70_4605-69insTTT...
ENST00000327475.10:c.4605-70_4605-69insTTTAT	ENSP00000333363.7:n.4605-70_4605-69insTTT...
ENST00000359357.7:c.3954-70_3954-69insTTTAT	ENSP00000352312.3:n.3954-70_3954-69insTTT...
ENST00000449981.6:c.4605-70_4605-69insTTTAT	ENSP00000415331.2:n.4605-70_4605-69insTTT...
NM_001206927.1:c.4605-70_4605-69insTTTAT	NP_001193856.1:n.4605-70_4605-69insTTTAT
XM_011514318.1:c.4542-70_4542-69insTTTAT	XP_011512620.1:n.4542-70_4542-69insTTTAT
XM_011514319.1:c.4605-70_4605-69insTTTAT	XP_011512621.1:n.4605-70_4605-69insTTTAT
XM_011514320.1:c.4368-70_4368-69insTTTAT	XP_011512622.1:n.4368-70_4368-69insTTTAT
XM_011514321.1:c.3954-70_3954-69insTTTAT	XP_011512623.1:n.3954-70_3954-69insTTTAT
XM_011514322.1:c.4605-70_4605-69insTTTAT	XP_011512624.1:n.4605-70_4605-69insTTTAT
XR_926078.1:n.4722-70_4722-69insTTTAT
NM_001371.3:c.3954-70_3954-69insTTTAT	NP_001362.2:n.3954-70_3954-69insTTTAT
XM_011514318.2:c.4542-70_4542-69insTTTAT	XP_011512620.1:n.4542-70_4542-69insTTTAT
XM_011514319.2:c.4605-70_4605-69insTTTAT	XP_011512621.1:n.4605-70_4605-69insTTTAT
XM_011514320.2:c.4368-70_4368-69insTTTAT	XP_011512622.1:n.4368-70_4368-69insTTTAT
XM_017010325.1:c.4605-70_4605-69insTTTAT	XP_016865814.1:n.4605-70_4605-69insTTTAT
XM_017010326.1:c.4605-70_4605-69insTTTAT	XP_016865815.1:n.4605-70_4605-69insTTTAT
XM_017010327.1:c.4605-70_4605-69insTTTAT	XP_016865816.1:n.4605-70_4605-69insTTTAT
XR_001743188.1:n.4726-70_4726-69insTTTAT
XR_926078.2:n.4725-70_4725-69insTTTAT
NM_001206927.2:c.4605-70_4605-69insTTTAT MANE Select	NP_001193856.1:n.4605-70_4605-69insTTTAT
NM_001371.4:c.3954-70_3954-69insTTTAT	NP_001362.2:n.3954-70_3954-69insTTTAT