Canonical Allele Identifier: CA443535807

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13753410-C-T
• MyVariant Identifiers: chr5:g.13753519C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753410C>T , CM000667.2:g.13753410C>T	GRCh38
NC_000005.9:g.13753519C>T , CM000667.1:g.13753519C>T	GRCh37
NC_000005.8:g.13806519C>T	NCBI36
NG_013081.1:g.196071G>A
NG_013081.2:g.196071G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10695G>A MANE Select	ENSP00000265104.4:p.Glu3565=
ENST00000681290.1:c.10650G>A	ENSP00000505288.1:p.Glu3550=
ENST00000265104.4:c.10695G>A	ENSP00000265104.4:p.Glu3565=
NM_001369.2:c.10695G>A	NP_001360.1:p.Glu3565=
XM_005248262.2:c.10650G>A	XP_005248319.1:p.Glu3550=
XM_005248262.3:c.10803G>A	XP_005248319.2:p.Glu3601=
XM_017009177.1:c.10803G>A	XP_016864666.1:p.Glu3601=
XM_017009178.1:c.9708G>A	XP_016864667.1:p.Glu3236=
XM_017009179.2:c.9708G>A	XP_016864668.1:p.Glu3236=
XM_017009180.1:c.10803G>A	XP_016864669.1:p.Glu3601=
XM_017009181.1:c.10803G>A	XP_016864670.1:p.Glu3601=
XM_017009182.1:c.10803G>A	XP_016864671.1:p.Glu3601=
XM_017009185.1:c.5892G>A	XP_016864674.1:p.Glu1964=
XM_017009186.1:c.5445G>A	XP_016864675.1:p.Glu1815=
XM_017009188.1:c.4782G>A	XP_016864677.1:p.Glu1594=
XM_024454388.1:c.9708G>A	XP_024310156.1:p.Glu3236=
XM_024454389.1:c.9297G>A	XP_024310157.1:p.Glu3099=
NM_001369.3:c.10695G>A MANE Select	NP_001360.1:p.Glu3565=