Canonical Allele Identifier: CA359212259

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13841949A>G (hg19) ; chr5:g.13841840A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13841840A>G , CM000667.2:g.13841840A>G	GRCh38
NC_000005.9:g.13841949A>G , CM000667.1:g.13841949A>G	GRCh37
NC_000005.8:g.13894949A>G	NCBI36
NG_013081.1:g.107641T>C
NG_013081.2:g.107641T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5336T>C MANE Select	ENSP00000265104.4:p.Val1779Ala
ENST00000681290.1:c.5291T>C	ENSP00000505288.1:p.Val1764Ala
ENST00000265104.4:c.5336T>C	ENSP00000265104.4:p.Val1779Ala
NM_001369.2:c.5336T>C	NP_001360.1:p.Val1779Ala
XM_005248262.2:c.5291T>C	XP_005248319.1:p.Val1764Ala
XM_011513990.1:c.5336T>C	XP_011512292.1:p.Val1779Ala
XR_925598.1:n.5543T>C
XM_005248262.3:c.5444T>C	XP_005248319.2:p.Val1815Ala
XM_017009177.1:c.5444T>C	XP_016864666.1:p.Val1815Ala
XM_017009178.1:c.4349T>C	XP_016864667.1:p.Val1450Ala
XM_017009179.2:c.4349T>C	XP_016864668.1:p.Val1450Ala
XM_017009180.1:c.5444T>C	XP_016864669.1:p.Val1815Ala
XM_017009181.1:c.5444T>C	XP_016864670.1:p.Val1815Ala
XM_017009182.1:c.5444T>C	XP_016864671.1:p.Val1815Ala
XM_017009183.1:c.5444T>C	XP_016864672.1:p.Val1815Ala
XM_017009184.1:c.5444T>C	XP_016864673.1:p.Val1815Ala
XM_017009185.1:c.533T>C	XP_016864674.1:p.Val178Ala
XM_017009186.1:c.86T>C	XP_016864675.1:p.Val29Ala
XM_017009187.1:c.5444T>C	XP_016864676.1:p.Val1815Ala
XM_024454388.1:c.4349T>C	XP_024310156.1:p.Val1450Ala
XM_024454389.1:c.3938T>C	XP_024310157.1:p.Val1313Ala
XR_001742034.1:n.5461T>C
XR_001742035.1:n.5461T>C
NM_001369.3:c.5336T>C MANE Select	NP_001360.1:p.Val1779Ala