Canonical Allele Identifier: CA443265782

Gene: DNAH5

Linked Data

• ClinVar Variation Id: 1092358
• ClinVar RCV Id: RCV001412156
• dbSNP Id: rs752656841
• gnomAD v3: 5-13793549-C-G
• gnomAD v4: 5-13793549-C-G
• MyVariant Identifiers: chr5:g.13793658C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793549C>G , CM000667.2:g.13793549C>G	GRCh38
NC_000005.9:g.13793658C>G , CM000667.1:g.13793658C>G	GRCh37
NC_000005.8:g.13846658C>G	NCBI36
NG_013081.1:g.155932G>C
NG_013081.2:g.155932G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.8190G>C MANE Select	ENSP00000265104.4:p.Thr2730=
ENST00000681290.1:c.8145G>C	ENSP00000505288.1:p.Thr2715=
ENST00000265104.4:c.8190G>C	ENSP00000265104.4:p.Thr2730=
NM_001369.2:c.8190G>C	NP_001360.1:p.Thr2730=
XM_005248262.2:c.8145G>C	XP_005248319.1:p.Thr2715=
XM_011513990.1:c.8190G>C	XP_011512292.1:p.Thr2730=
XR_925598.1:n.8397G>C
XM_005248262.3:c.8298G>C	XP_005248319.2:p.Thr2766=
XM_017009177.1:c.8298G>C	XP_016864666.1:p.Thr2766=
XM_017009178.1:c.7203G>C	XP_016864667.1:p.Thr2401=
XM_017009179.2:c.7203G>C	XP_016864668.1:p.Thr2401=
XM_017009180.1:c.8298G>C	XP_016864669.1:p.Thr2766=
XM_017009181.1:c.8298G>C	XP_016864670.1:p.Thr2766=
XM_017009182.1:c.8298G>C	XP_016864671.1:p.Thr2766=
XM_017009183.1:c.8298G>C	XP_016864672.1:p.Thr2766=
XM_017009184.1:c.8298G>C	XP_016864673.1:p.Thr2766=
XM_017009185.1:c.3387G>C	XP_016864674.1:p.Thr1129=
XM_017009186.1:c.2940G>C	XP_016864675.1:p.Thr980=
XM_017009188.1:c.2277G>C	XP_016864677.1:p.Thr759=
XM_024454388.1:c.7203G>C	XP_024310156.1:p.Thr2401=
XM_024454389.1:c.6792G>C	XP_024310157.1:p.Thr2264=
XR_001742034.1:n.8315G>C
XR_001742035.1:n.8315G>C
NM_001369.3:c.8190G>C MANE Select	NP_001360.1:p.Thr2730=