Canonical Allele Identifier: CA113919097

Gene: DNAH5

Linked Data

• dbSNP Id: rs1024588577
• MyVariant Identifiers: chr5:g.13753578A>G (hg19) ; chr5:g.13753469A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753469A>G , CM000667.2:g.13753469A>G	GRCh38
NC_000005.9:g.13753578A>G , CM000667.1:g.13753578A>G	GRCh37
NC_000005.8:g.13806578A>G	NCBI36
NG_013081.1:g.196012T>C
NG_013081.2:g.196012T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.10636T>C MANE Select	ENSP00000265104.4:p.Trp3546Arg
ENST00000681290.1:c.10591T>C	ENSP00000505288.1:p.Trp3531Arg
ENST00000265104.4:c.10636T>C	ENSP00000265104.4:p.Trp3546Arg
NM_001369.2:c.10636T>C	NP_001360.1:p.Trp3546Arg
XM_005248262.2:c.10591T>C	XP_005248319.1:p.Trp3531Arg
XM_005248262.3:c.10744T>C	XP_005248319.2:p.Trp3582Arg
XM_017009177.1:c.10744T>C	XP_016864666.1:p.Trp3582Arg
XM_017009178.1:c.9649T>C	XP_016864667.1:p.Trp3217Arg
XM_017009179.2:c.9649T>C	XP_016864668.1:p.Trp3217Arg
XM_017009180.1:c.10744T>C	XP_016864669.1:p.Trp3582Arg
XM_017009181.1:c.10744T>C	XP_016864670.1:p.Trp3582Arg
XM_017009182.1:c.10744T>C	XP_016864671.1:p.Trp3582Arg
XM_017009185.1:c.5833T>C	XP_016864674.1:p.Trp1945Arg
XM_017009186.1:c.5386T>C	XP_016864675.1:p.Trp1796Arg
XM_017009188.1:c.4723T>C	XP_016864677.1:p.Trp1575Arg
XM_024454388.1:c.9649T>C	XP_024310156.1:p.Trp3217Arg
XM_024454389.1:c.9238T>C	XP_024310157.1:p.Trp3080Arg
NM_001369.3:c.10636T>C MANE Select	NP_001360.1:p.Trp3546Arg