Canonical Allele Identifier: CA359231844

Gene: DNAH5

Linked Data

• dbSNP Id: rs1769994742
• MyVariant Identifiers: chr5:g.13870980T>G (hg19) ; chr5:g.13870871T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13870871T>G , CM000667.2:g.13870871T>G	GRCh38
NC_000005.9:g.13870980T>G , CM000667.1:g.13870980T>G	GRCh37
NC_000005.8:g.13923980T>G	NCBI36
NG_013081.1:g.78610A>C
NG_013081.2:g.78610A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.3730A>C MANE Select	ENSP00000265104.4:p.Asn1244His
ENST00000681290.1:c.3685A>C	ENSP00000505288.1:p.Asn1229His
ENST00000265104.4:c.3730A>C	ENSP00000265104.4:p.Asn1244His
NM_001369.2:c.3730A>C	NP_001360.1:p.Asn1244His
XM_005248262.2:c.3685A>C	XP_005248319.1:p.Asn1229His
XM_011513990.1:c.3730A>C	XP_011512292.1:p.Asn1244His
XR_925598.1:n.3937A>C
XM_005248262.3:c.3838A>C	XP_005248319.2:p.Asn1280His
XM_017009177.1:c.3838A>C	XP_016864666.1:p.Asn1280His
XM_017009178.1:c.2743A>C	XP_016864667.1:p.Asn915His
XM_017009179.2:c.2743A>C	XP_016864668.1:p.Asn915His
XM_017009180.1:c.3838A>C	XP_016864669.1:p.Asn1280His
XM_017009181.1:c.3838A>C	XP_016864670.1:p.Asn1280His
XM_017009182.1:c.3838A>C	XP_016864671.1:p.Asn1280His
XM_017009183.1:c.3838A>C	XP_016864672.1:p.Asn1280His
XM_017009184.1:c.3838A>C	XP_016864673.1:p.Asn1280His
XM_017009187.1:c.3838A>C	XP_016864676.1:p.Asn1280His
XM_024454388.1:c.2743A>C	XP_024310156.1:p.Asn915His
XM_024454389.1:c.2332A>C	XP_024310157.1:p.Asn778His
XR_001742034.1:n.3855A>C
XR_001742035.1:n.3855A>C
NM_001369.3:c.3730A>C MANE Select	NP_001360.1:p.Asn1244His