Canonical Allele Identifier: CA3203606
Community Standard Title: NM_001369.3(DNAH5):c.5692G>A (p.Asp1898Asn)
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13840923C>T , CM000667.2:g.13840923C>T GRCh38
NC_000005.9:g.13841032C>T , CM000667.1:g.13841032C>T GRCh37
NC_000005.8:g.13894032C>T NCBI36
NG_013081.1:g.108558G>A
NG_013081.2:g.108558G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001369.3:c.5692G>A MANE Select NP_001360.1:p.Asp1898Asn
ENST00000265104.5:c.5692G>A MANE Select ENSP00000265104.4:p.Asp1898Asn
NM_001369.2:c.5692G>A NP_001360.1:p.Asp1898Asn
ENST00000265104.4:c.5692G>A ENSP00000265104.4:p.Asp1898Asn
ENST00000681290.1:c.5647G>A ENSP00000505288.1:p.Asp1883Asn
XM_005248262.2:c.5647G>A XP_005248319.1:p.Asp1883Asn
XM_005248262.3:c.5800G>A XP_005248319.2:p.Asp1934Asn
XM_011513990.1:c.5692G>A XP_011512292.1:p.Asp1898Asn
XM_017009177.1:c.5800G>A XP_016864666.1:p.Asp1934Asn
XM_017009178.1:c.4705G>A XP_016864667.1:p.Asp1569Asn
XM_017009179.2:c.4705G>A XP_016864668.1:p.Asp1569Asn
XM_017009180.1:c.5800G>A XP_016864669.1:p.Asp1934Asn
XM_017009181.1:c.5800G>A XP_016864670.1:p.Asp1934Asn
XM_017009182.1:c.5800G>A XP_016864671.1:p.Asp1934Asn
XM_017009183.1:c.5800G>A XP_016864672.1:p.Asp1934Asn
XM_017009184.1:c.5800G>A XP_016864673.1:p.Asp1934Asn
XM_017009185.1:c.889G>A XP_016864674.1:p.Asp297Asn
XM_017009186.1:c.442G>A XP_016864675.1:p.Asp148Asn
XM_017009187.1:c.5800G>A XP_016864676.1:p.Asp1934Asn
XM_024454388.1:c.4705G>A XP_024310156.1:p.Asp1569Asn
XM_024454389.1:c.4294G>A XP_024310157.1:p.Asp1432Asn
XR_001742034.1:n.5817G>A
XR_001742035.1:n.5817G>A
XR_925598.1:n.5899G>A