Canonical Allele Identifier: CA359221070

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13793665T>C (hg19) ; chr5:g.13793556T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793556T>C , CM000667.2:g.13793556T>C	GRCh38
NC_000005.9:g.13793665T>C , CM000667.1:g.13793665T>C	GRCh37
NC_000005.8:g.13846665T>C	NCBI36
NG_013081.1:g.155925A>G
NG_013081.2:g.155925A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8183A>G MANE Select	ENSP00000265104.4:p.Asn2728Ser
ENST00000681290.1:c.8138A>G	ENSP00000505288.1:p.Asn2713Ser
ENST00000265104.4:c.8183A>G	ENSP00000265104.4:p.Asn2728Ser
NM_001369.2:c.8183A>G	NP_001360.1:p.Asn2728Ser
XM_005248262.2:c.8138A>G	XP_005248319.1:p.Asn2713Ser
XM_011513990.1:c.8183A>G	XP_011512292.1:p.Asn2728Ser
XR_925598.1:n.8390A>G
XM_005248262.3:c.8291A>G	XP_005248319.2:p.Asn2764Ser
XM_017009177.1:c.8291A>G	XP_016864666.1:p.Asn2764Ser
XM_017009178.1:c.7196A>G	XP_016864667.1:p.Asn2399Ser
XM_017009179.2:c.7196A>G	XP_016864668.1:p.Asn2399Ser
XM_017009180.1:c.8291A>G	XP_016864669.1:p.Asn2764Ser
XM_017009181.1:c.8291A>G	XP_016864670.1:p.Asn2764Ser
XM_017009182.1:c.8291A>G	XP_016864671.1:p.Asn2764Ser
XM_017009183.1:c.8291A>G	XP_016864672.1:p.Asn2764Ser
XM_017009184.1:c.8291A>G	XP_016864673.1:p.Asn2764Ser
XM_017009185.1:c.3380A>G	XP_016864674.1:p.Asn1127Ser
XM_017009186.1:c.2933A>G	XP_016864675.1:p.Asn978Ser
XM_017009188.1:c.2270A>G	XP_016864677.1:p.Asn757Ser
XM_024454388.1:c.7196A>G	XP_024310156.1:p.Asn2399Ser
XM_024454389.1:c.6785A>G	XP_024310157.1:p.Asn2262Ser
XR_001742034.1:n.8308A>G
XR_001742035.1:n.8308A>G
NM_001369.3:c.8183A>G MANE Select	NP_001360.1:p.Asn2728Ser