Canonical Allele Identifier: CA359213923

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13844987T>G (hg19) ; chr5:g.13844878T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13844878T>G , CM000667.2:g.13844878T>G	GRCh38
NC_000005.9:g.13844987T>G , CM000667.1:g.13844987T>G	GRCh37
NC_000005.8:g.13897987T>G	NCBI36
NG_013081.1:g.104603A>C
NG_013081.2:g.104603A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5230A>C MANE Select	ENSP00000265104.4:p.Asn1744His
ENST00000681290.1:c.5185A>C	ENSP00000505288.1:p.Asn1729His
ENST00000265104.4:c.5230A>C	ENSP00000265104.4:p.Asn1744His
NM_001369.2:c.5230A>C	NP_001360.1:p.Asn1744His
XM_005248262.2:c.5185A>C	XP_005248319.1:p.Asn1729His
XM_011513990.1:c.5230A>C	XP_011512292.1:p.Asn1744His
XR_925598.1:n.5437A>C
XM_005248262.3:c.5338A>C	XP_005248319.2:p.Asn1780His
XM_017009177.1:c.5338A>C	XP_016864666.1:p.Asn1780His
XM_017009178.1:c.4243A>C	XP_016864667.1:p.Asn1415His
XM_017009179.2:c.4243A>C	XP_016864668.1:p.Asn1415His
XM_017009180.1:c.5338A>C	XP_016864669.1:p.Asn1780His
XM_017009181.1:c.5338A>C	XP_016864670.1:p.Asn1780His
XM_017009182.1:c.5338A>C	XP_016864671.1:p.Asn1780His
XM_017009183.1:c.5338A>C	XP_016864672.1:p.Asn1780His
XM_017009184.1:c.5338A>C	XP_016864673.1:p.Asn1780His
XM_017009185.1:c.427A>C	XP_016864674.1:p.Asn143His
XM_017009186.1:c.22-2974A>C	XP_016864675.1:n.22-2974A>C
XM_017009187.1:c.5338A>C	XP_016864676.1:p.Asn1780His
XM_024454388.1:c.4243A>C	XP_024310156.1:p.Asn1415His
XM_024454389.1:c.3832A>C	XP_024310157.1:p.Asn1278His
XR_001742034.1:n.5355A>C
XR_001742035.1:n.5355A>C
NM_001369.3:c.5230A>C MANE Select	NP_001360.1:p.Asn1744His