Canonical Allele Identifier: CA3202943

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793979A>G , CM000667.2:g.13793979A>G	GRCh38
NC_000005.9:g.13794088A>G , CM000667.1:g.13794088A>G	GRCh37
NC_000005.8:g.13847088A>G	NCBI36
NG_013081.1:g.155502T>C
NG_013081.2:g.155502T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.7967T>C MANE Select	NP_001360.1:p.Ile2656Thr
ENST00000265104.5:c.7967T>C MANE Select	ENSP00000265104.4:p.Ile2656Thr
NM_001369.2:c.7967T>C	NP_001360.1:p.Ile2656Thr
ENST00000265104.4:c.7967T>C	ENSP00000265104.4:p.Ile2656Thr
ENST00000681290.1:c.7922T>C	ENSP00000505288.1:p.Ile2641Thr
XM_005248262.2:c.7922T>C	XP_005248319.1:p.Ile2641Thr
XM_005248262.3:c.8075T>C	XP_005248319.2:p.Ile2692Thr
XM_011513990.1:c.7967T>C	XP_011512292.1:p.Ile2656Thr
XM_017009177.1:c.8075T>C	XP_016864666.1:p.Ile2692Thr
XM_017009178.1:c.6980T>C	XP_016864667.1:p.Ile2327Thr
XM_017009179.2:c.6980T>C	XP_016864668.1:p.Ile2327Thr
XM_017009180.1:c.8075T>C	XP_016864669.1:p.Ile2692Thr
XM_017009181.1:c.8075T>C	XP_016864670.1:p.Ile2692Thr
XM_017009182.1:c.8075T>C	XP_016864671.1:p.Ile2692Thr
XM_017009183.1:c.8075T>C	XP_016864672.1:p.Ile2692Thr
XM_017009184.1:c.8075T>C	XP_016864673.1:p.Ile2692Thr
XM_017009185.1:c.3164T>C	XP_016864674.1:p.Ile1055Thr
XM_017009186.1:c.2717T>C	XP_016864675.1:p.Ile906Thr
XM_017009187.1:c.*70T>C	XP_016864676.1:n.*70T>C
XM_017009188.1:c.2054T>C	XP_016864677.1:p.Ile685Thr
XM_024454388.1:c.6980T>C	XP_024310156.1:p.Ile2327Thr
XM_024454389.1:c.6569T>C	XP_024310157.1:p.Ile2190Thr
XR_001742034.1:n.8092T>C
XR_001742035.1:n.8092T>C
XR_925598.1:n.8174T>C