Canonical Allele Identifier: CA2640179759

Gene: DNAH17

Linked Data

• gnomAD v4: 17-78566972-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78566972T>G , CM000679.2:g.78566972T>G	GRCh38
NC_000017.10:g.76563054T>G , CM000679.1:g.76563054T>G	GRCh37
NC_000017.9:g.74074649T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389840.7:c.1452+27A>C MANE Select	ENSP00000374490.6:n.1452+27A>C
ENST00000389840.6:c.1452+27A>C	ENSP00000374490.6:n.1452+27A>C
ENST00000585328.5:c.1452+27A>C	ENSP00000465516.1:n.1452+27A>C
ENST00000589793.1:n.664+27A>C
NM_173628.3:c.1452+27A>C	NP_775899.3:n.1452+27A>C
XM_011525416.1:c.1452+27A>C	XP_011523718.1:n.1452+27A>C
XM_011525417.1:c.1452+27A>C	XP_011523719.1:n.1452+27A>C
XR_934583.1:n.1613+27A>C
XM_011525416.2:c.1452+27A>C	XP_011523718.1:n.1452+27A>C
XM_024451013.1:c.1452+27A>C	XP_024306781.1:n.1452+27A>C
XM_024451014.1:c.1452+27A>C	XP_024306782.1:n.1452+27A>C
XR_002958080.1:n.1615+27A>C
XR_002958081.1:n.1619+27A>C
NM_173628.4:c.1452+27A>C MANE Select	NP_775899.3:n.1452+27A>C