Canonical Allele Identifier: CA443253662

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13769105T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13768996T>G , CM000667.2:g.13768996T>G	GRCh38
NC_000005.9:g.13769105T>G , CM000667.1:g.13769105T>G	GRCh37
NC_000005.8:g.13822105T>G	NCBI36
NG_013081.1:g.180485A>C
NG_013081.2:g.180485A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9861A>C MANE Select	ENSP00000265104.4:p.Ala3287=
ENST00000681290.1:c.9816A>C	ENSP00000505288.1:p.Ala3272=
ENST00000265104.4:c.9861A>C	ENSP00000265104.4:p.Ala3287=
ENST00000504001.3:n.573A>C
NM_001369.2:c.9861A>C	NP_001360.1:p.Ala3287=
XM_005248262.2:c.9816A>C	XP_005248319.1:p.Ala3272=
XM_005248262.3:c.9969A>C	XP_005248319.2:p.Ala3323=
XM_017009177.1:c.9969A>C	XP_016864666.1:p.Ala3323=
XM_017009178.1:c.8874A>C	XP_016864667.1:p.Ala2958=
XM_017009179.2:c.8874A>C	XP_016864668.1:p.Ala2958=
XM_017009180.1:c.9969A>C	XP_016864669.1:p.Ala3323=
XM_017009181.1:c.9969A>C	XP_016864670.1:p.Ala3323=
XM_017009182.1:c.9969A>C	XP_016864671.1:p.Ala3323=
XM_017009185.1:c.5058A>C	XP_016864674.1:p.Ala1686=
XM_017009186.1:c.4611A>C	XP_016864675.1:p.Ala1537=
XM_017009188.1:c.3948A>C	XP_016864677.1:p.Ala1316=
XM_024454388.1:c.8874A>C	XP_024310156.1:p.Ala2958=
XM_024454389.1:c.8463A>C	XP_024310157.1:p.Ala2821=
NM_001369.3:c.9861A>C MANE Select	NP_001360.1:p.Ala3287=