Canonical Allele Identifier: CA443535832

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13776804T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776695T>G , CM000667.2:g.13776695T>G	GRCh38
NC_000005.9:g.13776804T>G , CM000667.1:g.13776804T>G	GRCh37
NC_000005.8:g.13829804T>G	NCBI36
NG_013081.1:g.172786A>C
NG_013081.2:g.172786A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9117A>C MANE Select	ENSP00000265104.4:p.Leu3039=
ENST00000681290.1:c.9072A>C	ENSP00000505288.1:p.Leu3024=
ENST00000265104.4:c.9117A>C	ENSP00000265104.4:p.Leu3039=
NM_001369.2:c.9117A>C	NP_001360.1:p.Leu3039=
XM_005248262.2:c.9072A>C	XP_005248319.1:p.Leu3024=
XM_011513990.1:c.*4A>C	XP_011512292.1:n.*4A>C
XR_925598.1:n.9188A>C
XM_005248262.3:c.9225A>C	XP_005248319.2:p.Leu3075=
XM_017009177.1:c.9225A>C	XP_016864666.1:p.Leu3075=
XM_017009178.1:c.8130A>C	XP_016864667.1:p.Leu2710=
XM_017009179.2:c.8130A>C	XP_016864668.1:p.Leu2710=
XM_017009180.1:c.9225A>C	XP_016864669.1:p.Leu3075=
XM_017009181.1:c.9225A>C	XP_016864670.1:p.Leu3075=
XM_017009182.1:c.9225A>C	XP_016864671.1:p.Leu3075=
XM_017009183.1:c.9225A>C	XP_016864672.1:p.Leu3075=
XM_017009184.1:c.*4A>C	XP_016864673.1:n.*4A>C
XM_017009185.1:c.4314A>C	XP_016864674.1:p.Leu1438=
XM_017009186.1:c.3867A>C	XP_016864675.1:p.Leu1289=
XM_017009188.1:c.3204A>C	XP_016864677.1:p.Leu1068=
XM_024454388.1:c.8130A>C	XP_024310156.1:p.Leu2710=
XM_024454389.1:c.7719A>C	XP_024310157.1:p.Leu2573=
XR_001742034.1:n.9111A>C
XR_001742035.1:n.9106A>C
NM_001369.3:c.9117A>C MANE Select	NP_001360.1:p.Leu3039=