Canonical Allele Identifier: CA359190077

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13752205-C-T
• MyVariant Identifiers: chr5:g.13752314C>T (hg19) ; chr5:g.13752205C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13752205C>T , CM000667.2:g.13752205C>T	GRCh38
NC_000005.9:g.13752314C>T , CM000667.1:g.13752314C>T	GRCh37
NC_000005.8:g.13805314C>T	NCBI36
NG_013081.1:g.197276G>A
NG_013081.2:g.197276G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10957G>A MANE Select	ENSP00000265104.4:p.Gly3653Arg
ENST00000681290.1:c.10912G>A	ENSP00000505288.1:p.Gly3638Arg
ENST00000265104.4:c.10957G>A	ENSP00000265104.4:p.Gly3653Arg
NM_001369.2:c.10957G>A	NP_001360.1:p.Gly3653Arg
XM_005248262.2:c.10912G>A	XP_005248319.1:p.Gly3638Arg
XM_005248262.3:c.11065G>A	XP_005248319.2:p.Gly3689Arg
XM_017009177.1:c.11065G>A	XP_016864666.1:p.Gly3689Arg
XM_017009178.1:c.9970G>A	XP_016864667.1:p.Gly3324Arg
XM_017009179.2:c.9970G>A	XP_016864668.1:p.Gly3324Arg
XM_017009180.1:c.11065G>A	XP_016864669.1:p.Gly3689Arg
XM_017009181.1:c.11065G>A	XP_016864670.1:p.Gly3689Arg
XM_017009182.1:c.11065G>A	XP_016864671.1:p.Gly3689Arg
XM_017009185.1:c.6154G>A	XP_016864674.1:p.Gly2052Arg
XM_017009186.1:c.5707G>A	XP_016864675.1:p.Gly1903Arg
XM_017009188.1:c.5044G>A	XP_016864677.1:p.Gly1682Arg
XM_024454388.1:c.9970G>A	XP_024310156.1:p.Gly3324Arg
XM_024454389.1:c.9559G>A	XP_024310157.1:p.Gly3187Arg
NM_001369.3:c.10957G>A MANE Select	NP_001360.1:p.Gly3653Arg