Canonical Allele Identifier: CA359188736

Gene: DNAH5

Linked Data

• COSMIC: COSM357368
• MyVariant Identifiers: chr5:g.13692218A>T (hg19) ; chr5:g.13692109A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13692109A>T , CM000667.2:g.13692109A>T	GRCh38
NC_000005.9:g.13692218A>T , CM000667.1:g.13692218A>T	GRCh37
NC_000005.8:g.13745218A>T	NCBI36
NG_013081.1:g.257372T>A
NG_013081.2:g.257372T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1083T>A
ENST00000265104.5:c.13750T>A MANE Select	ENSP00000265104.4:p.Cys4584Ser
ENST00000681290.1:c.13705T>A	ENSP00000505288.1:p.Cys4569Ser
ENST00000265104.4:c.13750T>A	ENSP00000265104.4:p.Cys4584Ser
NM_001369.2:c.13750T>A	NP_001360.1:p.Cys4584Ser
XM_005248262.2:c.13705T>A	XP_005248319.1:p.Cys4569Ser
XM_005248262.3:c.13858T>A	XP_005248319.2:p.Cys4620Ser
XM_017009177.1:c.13438T>A	XP_016864666.1:p.Cys4480Ser
XM_017009178.1:c.12763T>A	XP_016864667.1:p.Cys4255Ser
XM_017009179.2:c.12763T>A	XP_016864668.1:p.Cys4255Ser
XM_017009185.1:c.8947T>A	XP_016864674.1:p.Cys2983Ser
XM_017009186.1:c.8500T>A	XP_016864675.1:p.Cys2834Ser
XM_017009188.1:c.7837T>A	XP_016864677.1:p.Cys2613Ser
XM_024454388.1:c.12763T>A	XP_024310156.1:p.Cys4255Ser
XM_024454389.1:c.12352T>A	XP_024310157.1:p.Cys4118Ser
NM_001369.3:c.13750T>A MANE Select	NP_001360.1:p.Cys4584Ser