Canonical Allele Identifier: CA443535601

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13770961G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13770852G>T , CM000667.2:g.13770852G>T	GRCh38
NC_000005.9:g.13770961G>T , CM000667.1:g.13770961G>T	GRCh37
NC_000005.8:g.13823961G>T	NCBI36
NG_013081.1:g.178629C>A
NG_013081.2:g.178629C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.9502C>A MANE Select	ENSP00000265104.4:p.Arg3168=
ENST00000681290.1:c.9457C>A	ENSP00000505288.1:p.Arg3153=
ENST00000265104.4:c.9502C>A	ENSP00000265104.4:p.Arg3168=
ENST00000504001.3:n.214C>A
NM_001369.2:c.9502C>A	NP_001360.1:p.Arg3168=
XM_005248262.2:c.9457C>A	XP_005248319.1:p.Arg3153=
XM_005248262.3:c.9610C>A	XP_005248319.2:p.Arg3204=
XM_017009177.1:c.9610C>A	XP_016864666.1:p.Arg3204=
XM_017009178.1:c.8515C>A	XP_016864667.1:p.Arg2839=
XM_017009179.2:c.8515C>A	XP_016864668.1:p.Arg2839=
XM_017009180.1:c.9610C>A	XP_016864669.1:p.Arg3204=
XM_017009181.1:c.9610C>A	XP_016864670.1:p.Arg3204=
XM_017009182.1:c.9610C>A	XP_016864671.1:p.Arg3204=
XM_017009183.1:c.9610C>A	XP_016864672.1:p.Arg3204=
XM_017009185.1:c.4699C>A	XP_016864674.1:p.Arg1567=
XM_017009186.1:c.4252C>A	XP_016864675.1:p.Arg1418=
XM_017009188.1:c.3589C>A	XP_016864677.1:p.Arg1197=
XM_024454388.1:c.8515C>A	XP_024310156.1:p.Arg2839=
XM_024454389.1:c.8104C>A	XP_024310157.1:p.Arg2702=
NM_001369.3:c.9502C>A MANE Select	NP_001360.1:p.Arg3168=