Canonical Allele Identifier: CA443535565

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13753477T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753368T>C , CM000667.2:g.13753368T>C	GRCh38
NC_000005.9:g.13753477T>C , CM000667.1:g.13753477T>C	GRCh37
NC_000005.8:g.13806477T>C	NCBI36
NG_013081.1:g.196113A>G
NG_013081.2:g.196113A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10737A>G MANE Select	ENSP00000265104.4:p.Gln3579=
ENST00000681290.1:c.10692A>G	ENSP00000505288.1:p.Gln3564=
ENST00000265104.4:c.10737A>G	ENSP00000265104.4:p.Gln3579=
NM_001369.2:c.10737A>G	NP_001360.1:p.Gln3579=
XM_005248262.2:c.10692A>G	XP_005248319.1:p.Gln3564=
XM_005248262.3:c.10845A>G	XP_005248319.2:p.Gln3615=
XM_017009177.1:c.10845A>G	XP_016864666.1:p.Gln3615=
XM_017009178.1:c.9750A>G	XP_016864667.1:p.Gln3250=
XM_017009179.2:c.9750A>G	XP_016864668.1:p.Gln3250=
XM_017009180.1:c.10845A>G	XP_016864669.1:p.Gln3615=
XM_017009181.1:c.10845A>G	XP_016864670.1:p.Gln3615=
XM_017009182.1:c.10845A>G	XP_016864671.1:p.Gln3615=
XM_017009185.1:c.5934A>G	XP_016864674.1:p.Gln1978=
XM_017009186.1:c.5487A>G	XP_016864675.1:p.Gln1829=
XM_017009188.1:c.4824A>G	XP_016864677.1:p.Gln1608=
XM_024454388.1:c.9750A>G	XP_024310156.1:p.Gln3250=
XM_024454389.1:c.9339A>G	XP_024310157.1:p.Gln3113=
NM_001369.3:c.10737A>G MANE Select	NP_001360.1:p.Gln3579=