Canonical Allele Identifier: CA986595405

Gene: DNAH17

Linked Data

• dbSNP Id: rs1598740868
• gnomAD v3: 17-78566980-A-C
• gnomAD v4: 17-78566980-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78566980A>C , CM000679.2:g.78566980A>C	GRCh38
NC_000017.10:g.76563062A>C , CM000679.1:g.76563062A>C	GRCh37
NC_000017.9:g.74074657A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389840.7:c.1452+19T>G MANE Select	ENSP00000374490.6:n.1452+19T>G
ENST00000389840.6:c.1452+19T>G	ENSP00000374490.6:n.1452+19T>G
ENST00000585328.5:c.1452+19T>G	ENSP00000465516.1:n.1452+19T>G
ENST00000589793.1:n.664+19T>G
NM_173628.3:c.1452+19T>G	NP_775899.3:n.1452+19T>G
XM_011525416.1:c.1452+19T>G	XP_011523718.1:n.1452+19T>G
XM_011525417.1:c.1452+19T>G	XP_011523719.1:n.1452+19T>G
XR_934583.1:n.1613+19T>G
XM_011525416.2:c.1452+19T>G	XP_011523718.1:n.1452+19T>G
XM_024451013.1:c.1452+19T>G	XP_024306781.1:n.1452+19T>G
XM_024451014.1:c.1452+19T>G	XP_024306782.1:n.1452+19T>G
XR_002958080.1:n.1615+19T>G
XR_002958081.1:n.1619+19T>G
NM_173628.4:c.1452+19T>G MANE Select	NP_775899.3:n.1452+19T>G