Canonical Allele Identifier: CA443259484

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13781057G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13780948G>C , CM000667.2:g.13780948G>C	GRCh38
NC_000005.9:g.13781057G>C , CM000667.1:g.13781057G>C	GRCh37
NC_000005.8:g.13834057G>C	NCBI36
NG_013081.1:g.168533C>G
NG_013081.2:g.168533C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8832C>G MANE Select	ENSP00000265104.4:p.Val2944=
ENST00000681290.1:c.8787C>G	ENSP00000505288.1:p.Val2929=
ENST00000265104.4:c.8832C>G	ENSP00000265104.4:p.Val2944=
NM_001369.2:c.8832C>G	NP_001360.1:p.Val2944=
XM_005248262.2:c.8787C>G	XP_005248319.1:p.Val2929=
XM_011513990.1:c.8832C>G	XP_011512292.1:p.Val2944=
XR_925598.1:n.9028-3593C>G
XM_005248262.3:c.8940C>G	XP_005248319.2:p.Val2980=
XM_017009177.1:c.8940C>G	XP_016864666.1:p.Val2980=
XM_017009178.1:c.7845C>G	XP_016864667.1:p.Val2615=
XM_017009179.2:c.7845C>G	XP_016864668.1:p.Val2615=
XM_017009180.1:c.8940C>G	XP_016864669.1:p.Val2980=
XM_017009181.1:c.8940C>G	XP_016864670.1:p.Val2980=
XM_017009182.1:c.8940C>G	XP_016864671.1:p.Val2980=
XM_017009183.1:c.8940C>G	XP_016864672.1:p.Val2980=
XM_017009184.1:c.8940C>G	XP_016864673.1:p.Val2980=
XM_017009185.1:c.4029C>G	XP_016864674.1:p.Val1343=
XM_017009186.1:c.3582C>G	XP_016864675.1:p.Val1194=
XM_017009188.1:c.2919C>G	XP_016864677.1:p.Val973=
XM_024454388.1:c.7845C>G	XP_024310156.1:p.Val2615=
XM_024454389.1:c.7434C>G	XP_024310157.1:p.Val2478=
XR_001742034.1:n.8946-3593C>G
XR_001742035.1:n.8946-3593C>G
NM_001369.3:c.8832C>G MANE Select	NP_001360.1:p.Val2944=