Canonical Allele Identifier: CA443265738

Gene: DNAH5

Linked Data

• ClinVar Variation Id: 1135408
• ClinVar RCV Id: RCV001470713
• dbSNP Id: rs1462731565
• gnomAD v2: 5-13793652-G-A
• gnomAD v4: 5-13793543-G-A
• MyVariant Identifiers: chr5:g.13793652G>A (hg19) ; chr5:g.13793543G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793543G>A , CM000667.2:g.13793543G>A	GRCh38
NC_000005.9:g.13793652G>A , CM000667.1:g.13793652G>A	GRCh37
NC_000005.8:g.13846652G>A	NCBI36
NG_013081.1:g.155938C>T
NG_013081.2:g.155938C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8196C>T MANE Select	ENSP00000265104.4:p.Pro2732=
ENST00000681290.1:c.8151C>T	ENSP00000505288.1:p.Pro2717=
ENST00000265104.4:c.8196C>T	ENSP00000265104.4:p.Pro2732=
NM_001369.2:c.8196C>T	NP_001360.1:p.Pro2732=
XM_005248262.2:c.8151C>T	XP_005248319.1:p.Pro2717=
XM_011513990.1:c.8196C>T	XP_011512292.1:p.Pro2732=
XR_925598.1:n.8403C>T
XM_005248262.3:c.8304C>T	XP_005248319.2:p.Pro2768=
XM_017009177.1:c.8304C>T	XP_016864666.1:p.Pro2768=
XM_017009178.1:c.7209C>T	XP_016864667.1:p.Pro2403=
XM_017009179.2:c.7209C>T	XP_016864668.1:p.Pro2403=
XM_017009180.1:c.8304C>T	XP_016864669.1:p.Pro2768=
XM_017009181.1:c.8304C>T	XP_016864670.1:p.Pro2768=
XM_017009182.1:c.8304C>T	XP_016864671.1:p.Pro2768=
XM_017009183.1:c.8304C>T	XP_016864672.1:p.Pro2768=
XM_017009184.1:c.8304C>T	XP_016864673.1:p.Pro2768=
XM_017009185.1:c.3393C>T	XP_016864674.1:p.Pro1131=
XM_017009186.1:c.2946C>T	XP_016864675.1:p.Pro982=
XM_017009188.1:c.2283C>T	XP_016864677.1:p.Pro761=
XM_024454388.1:c.7209C>T	XP_024310156.1:p.Pro2403=
XM_024454389.1:c.6798C>T	XP_024310157.1:p.Pro2266=
XR_001742034.1:n.8321C>T
XR_001742035.1:n.8321C>T
NM_001369.3:c.8196C>T MANE Select	NP_001360.1:p.Pro2732=