Canonical Allele Identifier: CA443535607

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13770965T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13770856T>C , CM000667.2:g.13770856T>C	GRCh38
NC_000005.9:g.13770965T>C , CM000667.1:g.13770965T>C	GRCh37
NC_000005.8:g.13823965T>C	NCBI36
NG_013081.1:g.178625A>G
NG_013081.2:g.178625A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.9498A>G MANE Select	ENSP00000265104.4:p.Arg3166=
ENST00000681290.1:c.9453A>G	ENSP00000505288.1:p.Arg3151=
ENST00000265104.4:c.9498A>G	ENSP00000265104.4:p.Arg3166=
ENST00000504001.3:n.210A>G
NM_001369.2:c.9498A>G	NP_001360.1:p.Arg3166=
XM_005248262.2:c.9453A>G	XP_005248319.1:p.Arg3151=
XM_005248262.3:c.9606A>G	XP_005248319.2:p.Arg3202=
XM_017009177.1:c.9606A>G	XP_016864666.1:p.Arg3202=
XM_017009178.1:c.8511A>G	XP_016864667.1:p.Arg2837=
XM_017009179.2:c.8511A>G	XP_016864668.1:p.Arg2837=
XM_017009180.1:c.9606A>G	XP_016864669.1:p.Arg3202=
XM_017009181.1:c.9606A>G	XP_016864670.1:p.Arg3202=
XM_017009182.1:c.9606A>G	XP_016864671.1:p.Arg3202=
XM_017009183.1:c.9606A>G	XP_016864672.1:p.Arg3202=
XM_017009185.1:c.4695A>G	XP_016864674.1:p.Arg1565=
XM_017009186.1:c.4248A>G	XP_016864675.1:p.Arg1416=
XM_017009188.1:c.3585A>G	XP_016864677.1:p.Arg1195=
XM_024454388.1:c.8511A>G	XP_024310156.1:p.Arg2837=
XM_024454389.1:c.8100A>G	XP_024310157.1:p.Arg2700=
NM_001369.3:c.9498A>G MANE Select	NP_001360.1:p.Arg3166=