Canonical Allele Identifier: CA359212672

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13780971G>A (hg19) ; chr5:g.13780862G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13780862G>A , CM000667.2:g.13780862G>A	GRCh38
NC_000005.9:g.13780971G>A , CM000667.1:g.13780971G>A	GRCh37
NC_000005.8:g.13833971G>A	NCBI36
NG_013081.1:g.168619C>T
NG_013081.2:g.168619C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.8918C>T MANE Select	ENSP00000265104.4:p.Ala2973Val
ENST00000681290.1:c.8873C>T	ENSP00000505288.1:p.Ala2958Val
ENST00000265104.4:c.8918C>T	ENSP00000265104.4:p.Ala2973Val
NM_001369.2:c.8918C>T	NP_001360.1:p.Ala2973Val
XM_005248262.2:c.8873C>T	XP_005248319.1:p.Ala2958Val
XM_011513990.1:c.8918C>T	XP_011512292.1:p.Ala2973Val
XR_925598.1:n.9028-3507C>T
XM_005248262.3:c.9026C>T	XP_005248319.2:p.Ala3009Val
XM_017009177.1:c.9026C>T	XP_016864666.1:p.Ala3009Val
XM_017009178.1:c.7931C>T	XP_016864667.1:p.Ala2644Val
XM_017009179.2:c.7931C>T	XP_016864668.1:p.Ala2644Val
XM_017009180.1:c.9026C>T	XP_016864669.1:p.Ala3009Val
XM_017009181.1:c.9026C>T	XP_016864670.1:p.Ala3009Val
XM_017009182.1:c.9026C>T	XP_016864671.1:p.Ala3009Val
XM_017009183.1:c.9026C>T	XP_016864672.1:p.Ala3009Val
XM_017009184.1:c.9026C>T	XP_016864673.1:p.Ala3009Val
XM_017009185.1:c.4115C>T	XP_016864674.1:p.Ala1372Val
XM_017009186.1:c.3668C>T	XP_016864675.1:p.Ala1223Val
XM_017009188.1:c.3005C>T	XP_016864677.1:p.Ala1002Val
XM_024454388.1:c.7931C>T	XP_024310156.1:p.Ala2644Val
XM_024454389.1:c.7520C>T	XP_024310157.1:p.Ala2507Val
XR_001742034.1:n.8946-3507C>T
XR_001742035.1:n.8946-3507C>T
NM_001369.3:c.8918C>T MANE Select	NP_001360.1:p.Ala2973Val