Canonical Allele Identifier: CA443248628

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13752282A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13752173A>G , CM000667.2:g.13752173A>G	GRCh38
NC_000005.9:g.13752282A>G , CM000667.1:g.13752282A>G	GRCh37
NC_000005.8:g.13805282A>G	NCBI36
NG_013081.1:g.197308T>C
NG_013081.2:g.197308T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10989T>C MANE Select	ENSP00000265104.4:p.Val3663=
ENST00000681290.1:c.10944T>C	ENSP00000505288.1:p.Val3648=
ENST00000265104.4:c.10989T>C	ENSP00000265104.4:p.Val3663=
NM_001369.2:c.10989T>C	NP_001360.1:p.Val3663=
XM_005248262.2:c.10944T>C	XP_005248319.1:p.Val3648=
XM_005248262.3:c.11097T>C	XP_005248319.2:p.Val3699=
XM_017009177.1:c.11097T>C	XP_016864666.1:p.Val3699=
XM_017009178.1:c.10002T>C	XP_016864667.1:p.Val3334=
XM_017009179.2:c.10002T>C	XP_016864668.1:p.Val3334=
XM_017009180.1:c.11097T>C	XP_016864669.1:p.Val3699=
XM_017009181.1:c.11097T>C	XP_016864670.1:p.Val3699=
XM_017009182.1:c.11097T>C	XP_016864671.1:p.Val3699=
XM_017009185.1:c.6186T>C	XP_016864674.1:p.Val2062=
XM_017009186.1:c.5739T>C	XP_016864675.1:p.Val1913=
XM_017009188.1:c.5076T>C	XP_016864677.1:p.Val1692=
XM_024454388.1:c.10002T>C	XP_024310156.1:p.Val3334=
XM_024454389.1:c.9591T>C	XP_024310157.1:p.Val3197=
NM_001369.3:c.10989T>C MANE Select	NP_001360.1:p.Val3663=