Canonical Allele Identifier: CA359192043

Gene: DNAH5

Linked Data

• dbSNP Id: rs1173924446
• gnomAD v2: 5-13753571-T-C
• gnomAD v4: 5-13753462-T-C
• MyVariant Identifiers: chr5:g.13753571T>C (hg19) ; chr5:g.13753462T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753462T>C , CM000667.2:g.13753462T>C	GRCh38
NC_000005.9:g.13753571T>C , CM000667.1:g.13753571T>C	GRCh37
NC_000005.8:g.13806571T>C	NCBI36
NG_013081.1:g.196019A>G
NG_013081.2:g.196019A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10643A>G MANE Select	ENSP00000265104.4:p.Lys3548Arg
ENST00000681290.1:c.10598A>G	ENSP00000505288.1:p.Lys3533Arg
ENST00000265104.4:c.10643A>G	ENSP00000265104.4:p.Lys3548Arg
NM_001369.2:c.10643A>G	NP_001360.1:p.Lys3548Arg
XM_005248262.2:c.10598A>G	XP_005248319.1:p.Lys3533Arg
XM_005248262.3:c.10751A>G	XP_005248319.2:p.Lys3584Arg
XM_017009177.1:c.10751A>G	XP_016864666.1:p.Lys3584Arg
XM_017009178.1:c.9656A>G	XP_016864667.1:p.Lys3219Arg
XM_017009179.2:c.9656A>G	XP_016864668.1:p.Lys3219Arg
XM_017009180.1:c.10751A>G	XP_016864669.1:p.Lys3584Arg
XM_017009181.1:c.10751A>G	XP_016864670.1:p.Lys3584Arg
XM_017009182.1:c.10751A>G	XP_016864671.1:p.Lys3584Arg
XM_017009185.1:c.5840A>G	XP_016864674.1:p.Lys1947Arg
XM_017009186.1:c.5393A>G	XP_016864675.1:p.Lys1798Arg
XM_017009188.1:c.4730A>G	XP_016864677.1:p.Lys1577Arg
XM_024454388.1:c.9656A>G	XP_024310156.1:p.Lys3219Arg
XM_024454389.1:c.9245A>G	XP_024310157.1:p.Lys3082Arg
NM_001369.3:c.10643A>G MANE Select	NP_001360.1:p.Lys3548Arg