Canonical Allele Identifier: CA443252728

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13830710A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13830601A>G , CM000667.2:g.13830601A>G	GRCh38
NC_000005.9:g.13830710A>G , CM000667.1:g.13830710A>G	GRCh37
NC_000005.8:g.13883710A>G	NCBI36
NG_013081.1:g.118880T>C
NG_013081.2:g.118880T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000683090.1:n.988T>C
ENST00000265104.5:c.6057T>C MANE Select	ENSP00000265104.4:p.Phe2019=
ENST00000681290.1:c.6012T>C	ENSP00000505288.1:p.Phe2004=
ENST00000265104.4:c.6057T>C	ENSP00000265104.4:p.Phe2019=
NM_001369.2:c.6057T>C	NP_001360.1:p.Phe2019=
XM_005248262.2:c.6012T>C	XP_005248319.1:p.Phe2004=
XM_011513990.1:c.6057T>C	XP_011512292.1:p.Phe2019=
XR_925598.1:n.6264T>C
XM_005248262.3:c.6165T>C	XP_005248319.2:p.Phe2055=
XM_017009177.1:c.6165T>C	XP_016864666.1:p.Phe2055=
XM_017009178.1:c.5070T>C	XP_016864667.1:p.Phe1690=
XM_017009179.2:c.5070T>C	XP_016864668.1:p.Phe1690=
XM_017009180.1:c.6165T>C	XP_016864669.1:p.Phe2055=
XM_017009181.1:c.6165T>C	XP_016864670.1:p.Phe2055=
XM_017009182.1:c.6165T>C	XP_016864671.1:p.Phe2055=
XM_017009183.1:c.6165T>C	XP_016864672.1:p.Phe2055=
XM_017009184.1:c.6165T>C	XP_016864673.1:p.Phe2055=
XM_017009185.1:c.1254T>C	XP_016864674.1:p.Phe418=
XM_017009186.1:c.807T>C	XP_016864675.1:p.Phe269=
XM_017009187.1:c.6165T>C	XP_016864676.1:p.Phe2055=
XM_017009188.1:c.144T>C	XP_016864677.1:p.Phe48=
XM_024454388.1:c.5070T>C	XP_024310156.1:p.Phe1690=
XM_024454389.1:c.4659T>C	XP_024310157.1:p.Phe1553=
XR_001742034.1:n.6182T>C
XR_001742035.1:n.6182T>C
NM_001369.3:c.6057T>C MANE Select	NP_001360.1:p.Phe2019=