Canonical Allele Identifier: CA359197037

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13708329A>T (hg19) ; chr5:g.13708220A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708220A>T , CM000667.2:g.13708220A>T	GRCh38
NC_000005.9:g.13708329A>T , CM000667.1:g.13708329A>T	GRCh37
NC_000005.8:g.13761329A>T	NCBI36
NG_013081.1:g.241261T>A
NG_013081.2:g.241261T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.574T>A
ENST00000265104.5:c.13241T>A MANE Select	ENSP00000265104.4:p.Leu4414Gln
ENST00000681290.1:c.13196T>A	ENSP00000505288.1:p.Leu4399Gln
ENST00000265104.4:c.13241T>A	ENSP00000265104.4:p.Leu4414Gln
NM_001369.2:c.13241T>A	NP_001360.1:p.Leu4414Gln
XM_005248262.2:c.13196T>A	XP_005248319.1:p.Leu4399Gln
XM_005248262.3:c.13349T>A	XP_005248319.2:p.Leu4450Gln
XM_017009177.1:c.12929T>A	XP_016864666.1:p.Leu4310Gln
XM_017009178.1:c.12254T>A	XP_016864667.1:p.Leu4085Gln
XM_017009179.2:c.12254T>A	XP_016864668.1:p.Leu4085Gln
XM_017009185.1:c.8438T>A	XP_016864674.1:p.Leu2813Gln
XM_017009186.1:c.7991T>A	XP_016864675.1:p.Leu2664Gln
XM_017009188.1:c.7328T>A	XP_016864677.1:p.Leu2443Gln
XM_024454388.1:c.12254T>A	XP_024310156.1:p.Leu4085Gln
XM_024454389.1:c.11843T>A	XP_024310157.1:p.Leu3948Gln
NM_001369.3:c.13241T>A MANE Select	NP_001360.1:p.Leu4414Gln