Canonical Allele Identifier: CA359199996

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13829581-T-C
• COSMIC: COSM3768148
• MyVariant Identifiers: chr5:g.13829690T>C (hg19) ; chr5:g.13829581T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13829581T>C , CM000667.2:g.13829581T>C	GRCh38
NC_000005.9:g.13829690T>C , CM000667.1:g.13829690T>C	GRCh37
NC_000005.8:g.13882690T>C	NCBI36
NG_013081.1:g.119900A>G
NG_013081.2:g.119900A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683090.1:n.1304A>G
ENST00000265104.5:c.6373A>G MANE Select	ENSP00000265104.4:p.Ile2125Val
ENST00000681290.1:c.6328A>G	ENSP00000505288.1:p.Ile2110Val
ENST00000265104.4:c.6373A>G	ENSP00000265104.4:p.Ile2125Val
NM_001369.2:c.6373A>G	NP_001360.1:p.Ile2125Val
XM_005248262.2:c.6328A>G	XP_005248319.1:p.Ile2110Val
XM_011513990.1:c.6373A>G	XP_011512292.1:p.Ile2125Val
XR_925598.1:n.6580A>G
XM_005248262.3:c.6481A>G	XP_005248319.2:p.Ile2161Val
XM_017009177.1:c.6481A>G	XP_016864666.1:p.Ile2161Val
XM_017009178.1:c.5386A>G	XP_016864667.1:p.Ile1796Val
XM_017009179.2:c.5386A>G	XP_016864668.1:p.Ile1796Val
XM_017009180.1:c.6481A>G	XP_016864669.1:p.Ile2161Val
XM_017009181.1:c.6481A>G	XP_016864670.1:p.Ile2161Val
XM_017009182.1:c.6481A>G	XP_016864671.1:p.Ile2161Val
XM_017009183.1:c.6481A>G	XP_016864672.1:p.Ile2161Val
XM_017009184.1:c.6481A>G	XP_016864673.1:p.Ile2161Val
XM_017009185.1:c.1570A>G	XP_016864674.1:p.Ile524Val
XM_017009186.1:c.1123A>G	XP_016864675.1:p.Ile375Val
XM_017009187.1:c.6481A>G	XP_016864676.1:p.Ile2161Val
XM_017009188.1:c.460A>G	XP_016864677.1:p.Ile154Val
XM_024454388.1:c.5386A>G	XP_024310156.1:p.Ile1796Val
XM_024454389.1:c.4975A>G	XP_024310157.1:p.Ile1659Val
XR_001742034.1:n.6498A>G
XR_001742035.1:n.6498A>G
NM_001369.3:c.6373A>G MANE Select	NP_001360.1:p.Ile2125Val