Canonical Allele Identifier: CA359204190

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13770775-A-C
• COSMIC: COSM5699320
• MyVariant Identifiers: chr5:g.13770884A>C (hg19) ; chr5:g.13770775A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13770775A>C , CM000667.2:g.13770775A>C	GRCh38
NC_000005.9:g.13770884A>C , CM000667.1:g.13770884A>C	GRCh37
NC_000005.8:g.13823884A>C	NCBI36
NG_013081.1:g.178706T>G
NG_013081.2:g.178706T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9579T>G MANE Select	ENSP00000265104.4:p.His3193Gln
ENST00000681290.1:c.9534T>G	ENSP00000505288.1:p.His3178Gln
ENST00000265104.4:c.9579T>G	ENSP00000265104.4:p.His3193Gln
ENST00000504001.3:n.291T>G
NM_001369.2:c.9579T>G	NP_001360.1:p.His3193Gln
XM_005248262.2:c.9534T>G	XP_005248319.1:p.His3178Gln
XM_005248262.3:c.9687T>G	XP_005248319.2:p.His3229Gln
XM_017009177.1:c.9687T>G	XP_016864666.1:p.His3229Gln
XM_017009178.1:c.8592T>G	XP_016864667.1:p.His2864Gln
XM_017009179.2:c.8592T>G	XP_016864668.1:p.His2864Gln
XM_017009180.1:c.9687T>G	XP_016864669.1:p.His3229Gln
XM_017009181.1:c.9687T>G	XP_016864670.1:p.His3229Gln
XM_017009182.1:c.9687T>G	XP_016864671.1:p.His3229Gln
XM_017009183.1:c.9687T>G	XP_016864672.1:p.His3229Gln
XM_017009185.1:c.4776T>G	XP_016864674.1:p.His1592Gln
XM_017009186.1:c.4329T>G	XP_016864675.1:p.His1443Gln
XM_017009188.1:c.3666T>G	XP_016864677.1:p.His1222Gln
XM_024454388.1:c.8592T>G	XP_024310156.1:p.His2864Gln
XM_024454389.1:c.8181T>G	XP_024310157.1:p.His2727Gln
NM_001369.3:c.9579T>G MANE Select	NP_001360.1:p.His3193Gln