Canonical Allele Identifier: CA359205389

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13771079G>T (hg19) ; chr5:g.13770970G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13770970G>T , CM000667.2:g.13770970G>T	GRCh38
NC_000005.9:g.13771079G>T , CM000667.1:g.13771079G>T	GRCh37
NC_000005.8:g.13824079G>T	NCBI36
NG_013081.1:g.178511C>A
NG_013081.2:g.178511C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9384C>A MANE Select	ENSP00000265104.4:p.His3128Gln
ENST00000681290.1:c.9339C>A	ENSP00000505288.1:p.His3113Gln
ENST00000265104.4:c.9384C>A	ENSP00000265104.4:p.His3128Gln
ENST00000504001.3:n.96C>A
NM_001369.2:c.9384C>A	NP_001360.1:p.His3128Gln
XM_005248262.2:c.9339C>A	XP_005248319.1:p.His3113Gln
XM_005248262.3:c.9492C>A	XP_005248319.2:p.His3164Gln
XM_017009177.1:c.9492C>A	XP_016864666.1:p.His3164Gln
XM_017009178.1:c.8397C>A	XP_016864667.1:p.His2799Gln
XM_017009179.2:c.8397C>A	XP_016864668.1:p.His2799Gln
XM_017009180.1:c.9492C>A	XP_016864669.1:p.His3164Gln
XM_017009181.1:c.9492C>A	XP_016864670.1:p.His3164Gln
XM_017009182.1:c.9492C>A	XP_016864671.1:p.His3164Gln
XM_017009183.1:c.9492C>A	XP_016864672.1:p.His3164Gln
XM_017009185.1:c.4581C>A	XP_016864674.1:p.His1527Gln
XM_017009186.1:c.4134C>A	XP_016864675.1:p.His1378Gln
XM_017009188.1:c.3471C>A	XP_016864677.1:p.His1157Gln
XM_024454388.1:c.8397C>A	XP_024310156.1:p.His2799Gln
XM_024454389.1:c.7986C>A	XP_024310157.1:p.His2662Gln
NM_001369.3:c.9384C>A MANE Select	NP_001360.1:p.His3128Gln