Canonical Allele Identifier: CA359199822

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13891198C>G (hg19) ; chr5:g.13891089C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13891089C>G , CM000667.2:g.13891089C>G	GRCh38
NC_000005.9:g.13891198C>G , CM000667.1:g.13891198C>G	GRCh37
NC_000005.8:g.13944198C>G	NCBI36
NG_013081.1:g.58392G>C
NG_013081.2:g.58392G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.2464G>C MANE Select	ENSP00000265104.4:p.Asp822His
ENST00000681290.1:c.2419G>C	ENSP00000505288.1:p.Asp807His
ENST00000265104.4:c.2464G>C	ENSP00000265104.4:p.Asp822His
NM_001369.2:c.2464G>C	NP_001360.1:p.Asp822His
XM_005248262.2:c.2419G>C	XP_005248319.1:p.Asp807His
XM_011513990.1:c.2464G>C	XP_011512292.1:p.Asp822His
XR_925598.1:n.2671G>C
XM_005248262.3:c.2572G>C	XP_005248319.2:p.Asp858His
XM_017009177.1:c.2572G>C	XP_016864666.1:p.Asp858His
XM_017009178.1:c.1477G>C	XP_016864667.1:p.Asp493His
XM_017009179.2:c.1477G>C	XP_016864668.1:p.Asp493His
XM_017009180.1:c.2572G>C	XP_016864669.1:p.Asp858His
XM_017009181.1:c.2572G>C	XP_016864670.1:p.Asp858His
XM_017009182.1:c.2572G>C	XP_016864671.1:p.Asp858His
XM_017009183.1:c.2572G>C	XP_016864672.1:p.Asp858His
XM_017009184.1:c.2572G>C	XP_016864673.1:p.Asp858His
XM_017009187.1:c.2572G>C	XP_016864676.1:p.Asp858His
XM_024454388.1:c.1477G>C	XP_024310156.1:p.Asp493His
XM_024454389.1:c.1066G>C	XP_024310157.1:p.Asp356His
XR_001742034.1:n.2589G>C
XR_001742035.1:n.2589G>C
NM_001369.3:c.2464G>C MANE Select	NP_001360.1:p.Asp822His