Canonical Allele Identifier: CA401286912

Gene: DNAH17

Linked Data

• gnomAD v4: 17-78567073-T-C
• MyVariant Identifiers: chr17:g.76563155T>C (hg19) ; chr17:g.78567073T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78567073T>C , CM000679.2:g.78567073T>C	GRCh38
NC_000017.10:g.76563155T>C , CM000679.1:g.76563155T>C	GRCh37
NC_000017.9:g.74074750T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389840.7:c.1378A>G MANE Select	ENSP00000374490.6:p.Ile460Val
ENST00000389840.6:c.1378A>G	ENSP00000374490.6:p.Ile460Val
ENST00000585328.5:c.1378A>G	ENSP00000465516.1:p.Ile460Val
ENST00000589793.1:n.590A>G
NM_173628.3:c.1378A>G	NP_775899.3:p.Ile460Val
XM_011525416.1:c.1378A>G	XP_011523718.1:p.Ile460Val
XM_011525417.1:c.1378A>G	XP_011523719.1:p.Ile460Val
XR_934583.1:n.1539A>G
XM_011525416.2:c.1378A>G	XP_011523718.1:p.Ile460Val
XM_024451013.1:c.1378A>G	XP_024306781.1:p.Ile460Val
XM_024451014.1:c.1378A>G	XP_024306782.1:p.Ile460Val
XR_002958080.1:n.1541A>G
XR_002958081.1:n.1545A>G
NM_173628.4:c.1378A>G MANE Select	NP_775899.3:p.Ile460Val