Canonical Allele Identifier: CA443273152

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13876922G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13876813G>T , CM000667.2:g.13876813G>T	GRCh38
NC_000005.9:g.13876922G>T , CM000667.1:g.13876922G>T	GRCh37
NC_000005.8:g.13929922G>T	NCBI36
NG_013081.1:g.72668C>A
NG_013081.2:g.72668C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.3267C>A MANE Select	ENSP00000265104.4:p.Thr1089=
ENST00000681290.1:c.3222C>A	ENSP00000505288.1:p.Thr1074=
ENST00000265104.4:c.3267C>A	ENSP00000265104.4:p.Thr1089=
NM_001369.2:c.3267C>A	NP_001360.1:p.Thr1089=
XM_005248262.2:c.3222C>A	XP_005248319.1:p.Thr1074=
XM_011513990.1:c.3267C>A	XP_011512292.1:p.Thr1089=
XR_925598.1:n.3474C>A
XM_005248262.3:c.3375C>A	XP_005248319.2:p.Thr1125=
XM_017009177.1:c.3375C>A	XP_016864666.1:p.Thr1125=
XM_017009178.1:c.2280C>A	XP_016864667.1:p.Thr760=
XM_017009179.2:c.2280C>A	XP_016864668.1:p.Thr760=
XM_017009180.1:c.3375C>A	XP_016864669.1:p.Thr1125=
XM_017009181.1:c.3375C>A	XP_016864670.1:p.Thr1125=
XM_017009182.1:c.3375C>A	XP_016864671.1:p.Thr1125=
XM_017009183.1:c.3375C>A	XP_016864672.1:p.Thr1125=
XM_017009184.1:c.3375C>A	XP_016864673.1:p.Thr1125=
XM_017009187.1:c.3375C>A	XP_016864676.1:p.Thr1125=
XM_024454388.1:c.2280C>A	XP_024310156.1:p.Thr760=
XM_024454389.1:c.1869C>A	XP_024310157.1:p.Thr623=
XR_001742034.1:n.3392C>A
XR_001742035.1:n.3392C>A
NM_001369.3:c.3267C>A MANE Select	NP_001360.1:p.Thr1089=