Canonical Allele Identifier: CA443535403

Gene: DNAH5

Linked Data

• ClinVar Variation Id: 2705766
• ClinVar RCV Id: RCV003536396
• MyVariant Identifiers: chr5:g.13753632G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753523G>A , CM000667.2:g.13753523G>A	GRCh38
NC_000005.9:g.13753632G>A , CM000667.1:g.13753632G>A	GRCh37
NC_000005.8:g.13806632G>A	NCBI36
NG_013081.1:g.195958C>T
NG_013081.2:g.195958C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10582C>T MANE Select	ENSP00000265104.4:p.Leu3528=
ENST00000681290.1:c.10537C>T	ENSP00000505288.1:p.Leu3513=
ENST00000265104.4:c.10582C>T	ENSP00000265104.4:p.Leu3528=
NM_001369.2:c.10582C>T	NP_001360.1:p.Leu3528=
XM_005248262.2:c.10537C>T	XP_005248319.1:p.Leu3513=
XM_005248262.3:c.10690C>T	XP_005248319.2:p.Leu3564=
XM_017009177.1:c.10690C>T	XP_016864666.1:p.Leu3564=
XM_017009178.1:c.9595C>T	XP_016864667.1:p.Leu3199=
XM_017009179.2:c.9595C>T	XP_016864668.1:p.Leu3199=
XM_017009180.1:c.10690C>T	XP_016864669.1:p.Leu3564=
XM_017009181.1:c.10690C>T	XP_016864670.1:p.Leu3564=
XM_017009182.1:c.10690C>T	XP_016864671.1:p.Leu3564=
XM_017009185.1:c.5779C>T	XP_016864674.1:p.Leu1927=
XM_017009186.1:c.5332C>T	XP_016864675.1:p.Leu1778=
XM_017009188.1:c.4669C>T	XP_016864677.1:p.Leu1557=
XM_024454388.1:c.9595C>T	XP_024310156.1:p.Leu3199=
XM_024454389.1:c.9184C>T	XP_024310157.1:p.Leu3062=
NM_001369.3:c.10582C>T MANE Select	NP_001360.1:p.Leu3528=