Canonical Allele Identifier: CA359202421

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13830752A>C (hg19) ; chr5:g.13830643A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13830643A>C , CM000667.2:g.13830643A>C	GRCh38
NC_000005.9:g.13830752A>C , CM000667.1:g.13830752A>C	GRCh37
NC_000005.8:g.13883752A>C	NCBI36
NG_013081.1:g.118838T>G
NG_013081.2:g.118838T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000683090.1:n.946T>G
ENST00000265104.5:c.6015T>G MANE Select	ENSP00000265104.4:p.Asn2005Lys
ENST00000681290.1:c.5970T>G	ENSP00000505288.1:p.Asn1990Lys
ENST00000265104.4:c.6015T>G	ENSP00000265104.4:p.Asn2005Lys
NM_001369.2:c.6015T>G	NP_001360.1:p.Asn2005Lys
XM_005248262.2:c.5970T>G	XP_005248319.1:p.Asn1990Lys
XM_011513990.1:c.6015T>G	XP_011512292.1:p.Asn2005Lys
XR_925598.1:n.6222T>G
XM_005248262.3:c.6123T>G	XP_005248319.2:p.Asn2041Lys
XM_017009177.1:c.6123T>G	XP_016864666.1:p.Asn2041Lys
XM_017009178.1:c.5028T>G	XP_016864667.1:p.Asn1676Lys
XM_017009179.2:c.5028T>G	XP_016864668.1:p.Asn1676Lys
XM_017009180.1:c.6123T>G	XP_016864669.1:p.Asn2041Lys
XM_017009181.1:c.6123T>G	XP_016864670.1:p.Asn2041Lys
XM_017009182.1:c.6123T>G	XP_016864671.1:p.Asn2041Lys
XM_017009183.1:c.6123T>G	XP_016864672.1:p.Asn2041Lys
XM_017009184.1:c.6123T>G	XP_016864673.1:p.Asn2041Lys
XM_017009185.1:c.1212T>G	XP_016864674.1:p.Asn404Lys
XM_017009186.1:c.765T>G	XP_016864675.1:p.Asn255Lys
XM_017009187.1:c.6123T>G	XP_016864676.1:p.Asn2041Lys
XM_017009188.1:c.102T>G	XP_016864677.1:p.Asn34Lys
XM_024454388.1:c.5028T>G	XP_024310156.1:p.Asn1676Lys
XM_024454389.1:c.4617T>G	XP_024310157.1:p.Asn1539Lys
XR_001742034.1:n.6140T>G
XR_001742035.1:n.6140T>G
NM_001369.3:c.6015T>G MANE Select	NP_001360.1:p.Asn2005Lys