Canonical Allele Identifier: CA443257730

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13844979A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13844870A>G , CM000667.2:g.13844870A>G	GRCh38
NC_000005.9:g.13844979A>G , CM000667.1:g.13844979A>G	GRCh37
NC_000005.8:g.13897979A>G	NCBI36
NG_013081.1:g.104611T>C
NG_013081.2:g.104611T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5238T>C MANE Select	ENSP00000265104.4:p.Phe1746=
ENST00000681290.1:c.5193T>C	ENSP00000505288.1:p.Phe1731=
ENST00000265104.4:c.5238T>C	ENSP00000265104.4:p.Phe1746=
NM_001369.2:c.5238T>C	NP_001360.1:p.Phe1746=
XM_005248262.2:c.5193T>C	XP_005248319.1:p.Phe1731=
XM_011513990.1:c.5238T>C	XP_011512292.1:p.Phe1746=
XR_925598.1:n.5445T>C
XM_005248262.3:c.5346T>C	XP_005248319.2:p.Phe1782=
XM_017009177.1:c.5346T>C	XP_016864666.1:p.Phe1782=
XM_017009178.1:c.4251T>C	XP_016864667.1:p.Phe1417=
XM_017009179.2:c.4251T>C	XP_016864668.1:p.Phe1417=
XM_017009180.1:c.5346T>C	XP_016864669.1:p.Phe1782=
XM_017009181.1:c.5346T>C	XP_016864670.1:p.Phe1782=
XM_017009182.1:c.5346T>C	XP_016864671.1:p.Phe1782=
XM_017009183.1:c.5346T>C	XP_016864672.1:p.Phe1782=
XM_017009184.1:c.5346T>C	XP_016864673.1:p.Phe1782=
XM_017009185.1:c.435T>C	XP_016864674.1:p.Phe145=
XM_017009186.1:c.22-2966T>C	XP_016864675.1:n.22-2966T>C
XM_017009187.1:c.5346T>C	XP_016864676.1:p.Phe1782=
XM_024454388.1:c.4251T>C	XP_024310156.1:p.Phe1417=
XM_024454389.1:c.3840T>C	XP_024310157.1:p.Phe1280=
XR_001742034.1:n.5363T>C
XR_001742035.1:n.5363T>C
NM_001369.3:c.5238T>C MANE Select	NP_001360.1:p.Phe1746=