Canonical Allele Identifier: CA359225209

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13736023A>C (hg19) ; chr5:g.13735914A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13735914A>C , CM000667.2:g.13735914A>C	GRCh38
NC_000005.9:g.13736023A>C , CM000667.1:g.13736023A>C	GRCh37
NC_000005.8:g.13789023A>C	NCBI36
NG_013081.1:g.213567T>G
NG_013081.2:g.213567T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.11474T>G MANE Select	ENSP00000265104.4:p.Ile3825Ser
ENST00000681290.1:c.11429T>G	ENSP00000505288.1:p.Ile3810Ser
ENST00000265104.4:c.11474T>G	ENSP00000265104.4:p.Ile3825Ser
NM_001369.2:c.11474T>G	NP_001360.1:p.Ile3825Ser
XM_005248262.2:c.11429T>G	XP_005248319.1:p.Ile3810Ser
XM_005248262.3:c.11582T>G	XP_005248319.2:p.Ile3861Ser
XM_017009177.1:c.11582T>G	XP_016864666.1:p.Ile3861Ser
XM_017009178.1:c.10487T>G	XP_016864667.1:p.Ile3496Ser
XM_017009179.2:c.10487T>G	XP_016864668.1:p.Ile3496Ser
XM_017009180.1:c.11582T>G	XP_016864669.1:p.Ile3861Ser
XM_017009181.1:c.11582T>G	XP_016864670.1:p.Ile3861Ser
XM_017009182.1:c.11338T>G	XP_016864671.1:p.Ser3780Ala
XM_017009185.1:c.6671T>G	XP_016864674.1:p.Ile2224Ser
XM_017009186.1:c.6224T>G	XP_016864675.1:p.Ile2075Ser
XM_017009188.1:c.5561T>G	XP_016864677.1:p.Ile1854Ser
XM_024454388.1:c.10487T>G	XP_024310156.1:p.Ile3496Ser
XM_024454389.1:c.10076T>G	XP_024310157.1:p.Ile3359Ser
NM_001369.3:c.11474T>G MANE Select	NP_001360.1:p.Ile3825Ser