Canonical Allele Identifier: CA359208468

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13776635G>C (hg19) ; chr5:g.13776526G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776526G>C , CM000667.2:g.13776526G>C	GRCh38
NC_000005.9:g.13776635G>C , CM000667.1:g.13776635G>C	GRCh37
NC_000005.8:g.13829635G>C	NCBI36
NG_013081.1:g.172955C>G
NG_013081.2:g.172955C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9286C>G MANE Select	ENSP00000265104.4:p.Arg3096Gly
ENST00000681290.1:c.9241C>G	ENSP00000505288.1:p.Arg3081Gly
ENST00000265104.4:c.9286C>G	ENSP00000265104.4:p.Arg3096Gly
NM_001369.2:c.9286C>G	NP_001360.1:p.Arg3096Gly
XM_005248262.2:c.9241C>G	XP_005248319.1:p.Arg3081Gly
XM_005248262.3:c.9394C>G	XP_005248319.2:p.Arg3132Gly
XM_017009177.1:c.9394C>G	XP_016864666.1:p.Arg3132Gly
XM_017009178.1:c.8299C>G	XP_016864667.1:p.Arg2767Gly
XM_017009179.2:c.8299C>G	XP_016864668.1:p.Arg2767Gly
XM_017009180.1:c.9394C>G	XP_016864669.1:p.Arg3132Gly
XM_017009181.1:c.9394C>G	XP_016864670.1:p.Arg3132Gly
XM_017009182.1:c.9394C>G	XP_016864671.1:p.Arg3132Gly
XM_017009183.1:c.9394C>G	XP_016864672.1:p.Arg3132Gly
XM_017009185.1:c.4483C>G	XP_016864674.1:p.Arg1495Gly
XM_017009186.1:c.4036C>G	XP_016864675.1:p.Arg1346Gly
XM_017009188.1:c.3373C>G	XP_016864677.1:p.Arg1125Gly
XM_024454388.1:c.8299C>G	XP_024310156.1:p.Arg2767Gly
XM_024454389.1:c.7888C>G	XP_024310157.1:p.Arg2630Gly
NM_001369.3:c.9286C>G MANE Select	NP_001360.1:p.Arg3096Gly