Canonical Allele Identifier: CA359188661

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13692182T>A (hg19) ; chr5:g.13692073T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13692073T>A , CM000667.2:g.13692073T>A	GRCh38
NC_000005.9:g.13692182T>A , CM000667.1:g.13692182T>A	GRCh37
NC_000005.8:g.13745182T>A	NCBI36
NG_013081.1:g.257408A>T
NG_013081.2:g.257408A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1119A>T
ENST00000265104.5:c.13786A>T MANE Select	ENSP00000265104.4:p.Asn4596Tyr
ENST00000681290.1:c.13741A>T	ENSP00000505288.1:p.Asn4581Tyr
ENST00000265104.4:c.13786A>T	ENSP00000265104.4:p.Asn4596Tyr
NM_001369.2:c.13786A>T	NP_001360.1:p.Asn4596Tyr
XM_005248262.2:c.13741A>T	XP_005248319.1:p.Asn4581Tyr
XM_005248262.3:c.13894A>T	XP_005248319.2:p.Asn4632Tyr
XM_017009177.1:c.13474A>T	XP_016864666.1:p.Asn4492Tyr
XM_017009178.1:c.12799A>T	XP_016864667.1:p.Asn4267Tyr
XM_017009179.2:c.12799A>T	XP_016864668.1:p.Asn4267Tyr
XM_017009185.1:c.8983A>T	XP_016864674.1:p.Asn2995Tyr
XM_017009186.1:c.8536A>T	XP_016864675.1:p.Asn2846Tyr
XM_017009188.1:c.7873A>T	XP_016864677.1:p.Asn2625Tyr
XM_024454388.1:c.12799A>T	XP_024310156.1:p.Asn4267Tyr
XM_024454389.1:c.12388A>T	XP_024310157.1:p.Asn4130Tyr
NM_001369.3:c.13786A>T MANE Select	NP_001360.1:p.Asn4596Tyr