Canonical Allele Identifier: CA359205419

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13771087A>T (hg19) ; chr5:g.13770978A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13770978A>T , CM000667.2:g.13770978A>T	GRCh38
NC_000005.9:g.13771087A>T , CM000667.1:g.13771087A>T	GRCh37
NC_000005.8:g.13824087A>T	NCBI36
NG_013081.1:g.178503T>A
NG_013081.2:g.178503T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9376T>A MANE Select	ENSP00000265104.4:p.Ser3126Thr
ENST00000681290.1:c.9331T>A	ENSP00000505288.1:p.Ser3111Thr
ENST00000265104.4:c.9376T>A	ENSP00000265104.4:p.Ser3126Thr
ENST00000504001.3:n.88T>A
NM_001369.2:c.9376T>A	NP_001360.1:p.Ser3126Thr
XM_005248262.2:c.9331T>A	XP_005248319.1:p.Ser3111Thr
XM_005248262.3:c.9484T>A	XP_005248319.2:p.Ser3162Thr
XM_017009177.1:c.9484T>A	XP_016864666.1:p.Ser3162Thr
XM_017009178.1:c.8389T>A	XP_016864667.1:p.Ser2797Thr
XM_017009179.2:c.8389T>A	XP_016864668.1:p.Ser2797Thr
XM_017009180.1:c.9484T>A	XP_016864669.1:p.Ser3162Thr
XM_017009181.1:c.9484T>A	XP_016864670.1:p.Ser3162Thr
XM_017009182.1:c.9484T>A	XP_016864671.1:p.Ser3162Thr
XM_017009183.1:c.9484T>A	XP_016864672.1:p.Ser3162Thr
XM_017009185.1:c.4573T>A	XP_016864674.1:p.Ser1525Thr
XM_017009186.1:c.4126T>A	XP_016864675.1:p.Ser1376Thr
XM_017009188.1:c.3463T>A	XP_016864677.1:p.Ser1155Thr
XM_024454388.1:c.8389T>A	XP_024310156.1:p.Ser2797Thr
XM_024454389.1:c.7978T>A	XP_024310157.1:p.Ser2660Thr
NM_001369.3:c.9376T>A MANE Select	NP_001360.1:p.Ser3126Thr