Canonical Allele Identifier: CA359232389

Gene: DNAH5

Linked Data

• ClinVar Variation Id: 1733291
• ClinVar RCV Id: RCV002452275
• gnomAD v4: 5-13870982-T-G
• MyVariant Identifiers: chr5:g.13871091T>G (hg19) ; chr5:g.13870982T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13870982T>G , CM000667.2:g.13870982T>G	GRCh38
NC_000005.9:g.13871091T>G , CM000667.1:g.13871091T>G	GRCh37
NC_000005.8:g.13924091T>G	NCBI36
NG_013081.1:g.78499A>C
NG_013081.2:g.78499A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.3619A>C MANE Select	ENSP00000265104.4:p.Thr1207Pro
ENST00000681290.1:c.3574A>C	ENSP00000505288.1:p.Thr1192Pro
ENST00000265104.4:c.3619A>C	ENSP00000265104.4:p.Thr1207Pro
NM_001369.2:c.3619A>C	NP_001360.1:p.Thr1207Pro
XM_005248262.2:c.3574A>C	XP_005248319.1:p.Thr1192Pro
XM_011513990.1:c.3619A>C	XP_011512292.1:p.Thr1207Pro
XR_925598.1:n.3826A>C
XM_005248262.3:c.3727A>C	XP_005248319.2:p.Thr1243Pro
XM_017009177.1:c.3727A>C	XP_016864666.1:p.Thr1243Pro
XM_017009178.1:c.2632A>C	XP_016864667.1:p.Thr878Pro
XM_017009179.2:c.2632A>C	XP_016864668.1:p.Thr878Pro
XM_017009180.1:c.3727A>C	XP_016864669.1:p.Thr1243Pro
XM_017009181.1:c.3727A>C	XP_016864670.1:p.Thr1243Pro
XM_017009182.1:c.3727A>C	XP_016864671.1:p.Thr1243Pro
XM_017009183.1:c.3727A>C	XP_016864672.1:p.Thr1243Pro
XM_017009184.1:c.3727A>C	XP_016864673.1:p.Thr1243Pro
XM_017009187.1:c.3727A>C	XP_016864676.1:p.Thr1243Pro
XM_024454388.1:c.2632A>C	XP_024310156.1:p.Thr878Pro
XM_024454389.1:c.2221A>C	XP_024310157.1:p.Thr741Pro
XR_001742034.1:n.3744A>C
XR_001742035.1:n.3744A>C
NM_001369.3:c.3619A>C MANE Select	NP_001360.1:p.Thr1207Pro