Canonical Allele Identifier: CA359205334

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13770960-A-T
• MyVariant Identifiers: chr5:g.13771069A>T (hg19) ; chr5:g.13770960A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13770960A>T , CM000667.2:g.13770960A>T	GRCh38
NC_000005.9:g.13771069A>T , CM000667.1:g.13771069A>T	GRCh37
NC_000005.8:g.13824069A>T	NCBI36
NG_013081.1:g.178521T>A
NG_013081.2:g.178521T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9394T>A MANE Select	ENSP00000265104.4:p.Ser3132Thr
ENST00000681290.1:c.9349T>A	ENSP00000505288.1:p.Ser3117Thr
ENST00000265104.4:c.9394T>A	ENSP00000265104.4:p.Ser3132Thr
ENST00000504001.3:n.106T>A
NM_001369.2:c.9394T>A	NP_001360.1:p.Ser3132Thr
XM_005248262.2:c.9349T>A	XP_005248319.1:p.Ser3117Thr
XM_005248262.3:c.9502T>A	XP_005248319.2:p.Ser3168Thr
XM_017009177.1:c.9502T>A	XP_016864666.1:p.Ser3168Thr
XM_017009178.1:c.8407T>A	XP_016864667.1:p.Ser2803Thr
XM_017009179.2:c.8407T>A	XP_016864668.1:p.Ser2803Thr
XM_017009180.1:c.9502T>A	XP_016864669.1:p.Ser3168Thr
XM_017009181.1:c.9502T>A	XP_016864670.1:p.Ser3168Thr
XM_017009182.1:c.9502T>A	XP_016864671.1:p.Ser3168Thr
XM_017009183.1:c.9502T>A	XP_016864672.1:p.Ser3168Thr
XM_017009185.1:c.4591T>A	XP_016864674.1:p.Ser1531Thr
XM_017009186.1:c.4144T>A	XP_016864675.1:p.Ser1382Thr
XM_017009188.1:c.3481T>A	XP_016864677.1:p.Ser1161Thr
XM_024454388.1:c.8407T>A	XP_024310156.1:p.Ser2803Thr
XM_024454389.1:c.7996T>A	XP_024310157.1:p.Ser2666Thr
NM_001369.3:c.9394T>A MANE Select	NP_001360.1:p.Ser3132Thr