Canonical Allele Identifier: CA359219205

Gene: DNAH5

Linked Data

• dbSNP Id: rs1757088601
• COSMIC: COSM3393159
• MyVariant Identifiers: chr5:g.13792200G>A (hg19) ; chr5:g.13792091G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13792091G>A , CM000667.2:g.13792091G>A	GRCh38
NC_000005.9:g.13792200G>A , CM000667.1:g.13792200G>A	GRCh37
NC_000005.8:g.13845200G>A	NCBI36
NG_013081.1:g.157390C>T
NG_013081.2:g.157390C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8351C>T MANE Select	ENSP00000265104.4:p.Thr2784Ile
ENST00000681290.1:c.8306C>T	ENSP00000505288.1:p.Thr2769Ile
ENST00000265104.4:c.8351C>T	ENSP00000265104.4:p.Thr2784Ile
NM_001369.2:c.8351C>T	NP_001360.1:p.Thr2784Ile
XM_005248262.2:c.8306C>T	XP_005248319.1:p.Thr2769Ile
XM_011513990.1:c.8351C>T	XP_011512292.1:p.Thr2784Ile
XR_925598.1:n.8558C>T
XM_005248262.3:c.8459C>T	XP_005248319.2:p.Thr2820Ile
XM_017009177.1:c.8459C>T	XP_016864666.1:p.Thr2820Ile
XM_017009178.1:c.7364C>T	XP_016864667.1:p.Thr2455Ile
XM_017009179.2:c.7364C>T	XP_016864668.1:p.Thr2455Ile
XM_017009180.1:c.8459C>T	XP_016864669.1:p.Thr2820Ile
XM_017009181.1:c.8459C>T	XP_016864670.1:p.Thr2820Ile
XM_017009182.1:c.8459C>T	XP_016864671.1:p.Thr2820Ile
XM_017009183.1:c.8459C>T	XP_016864672.1:p.Thr2820Ile
XM_017009184.1:c.8459C>T	XP_016864673.1:p.Thr2820Ile
XM_017009185.1:c.3548C>T	XP_016864674.1:p.Thr1183Ile
XM_017009186.1:c.3101C>T	XP_016864675.1:p.Thr1034Ile
XM_017009188.1:c.2438C>T	XP_016864677.1:p.Thr813Ile
XM_024454388.1:c.7364C>T	XP_024310156.1:p.Thr2455Ile
XM_024454389.1:c.6953C>T	XP_024310157.1:p.Thr2318Ile
XR_001742034.1:n.8476C>T
XR_001742035.1:n.8476C>T
NM_001369.3:c.8351C>T MANE Select	NP_001360.1:p.Thr2784Ile