Canonical Allele Identifier: CA443251319

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13708366T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708257T>G , CM000667.2:g.13708257T>G	GRCh38
NC_000005.9:g.13708366T>G , CM000667.1:g.13708366T>G	GRCh37
NC_000005.8:g.13761366T>G	NCBI36
NG_013081.1:g.241224A>C
NG_013081.2:g.241224A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.537A>C
ENST00000265104.5:c.13204A>C MANE Select	ENSP00000265104.4:p.Arg4402=
ENST00000681290.1:c.13159A>C	ENSP00000505288.1:p.Arg4387=
ENST00000265104.4:c.13204A>C	ENSP00000265104.4:p.Arg4402=
NM_001369.2:c.13204A>C	NP_001360.1:p.Arg4402=
XM_005248262.2:c.13159A>C	XP_005248319.1:p.Arg4387=
XM_005248262.3:c.13312A>C	XP_005248319.2:p.Arg4438=
XM_017009177.1:c.12892A>C	XP_016864666.1:p.Arg4298=
XM_017009178.1:c.12217A>C	XP_016864667.1:p.Arg4073=
XM_017009179.2:c.12217A>C	XP_016864668.1:p.Arg4073=
XM_017009185.1:c.8401A>C	XP_016864674.1:p.Arg2801=
XM_017009186.1:c.7954A>C	XP_016864675.1:p.Arg2652=
XM_017009188.1:c.7291A>C	XP_016864677.1:p.Arg2431=
XM_024454388.1:c.12217A>C	XP_024310156.1:p.Arg4073=
XM_024454389.1:c.11806A>C	XP_024310157.1:p.Arg3936=
NM_001369.3:c.13204A>C MANE Select	NP_001360.1:p.Arg4402=