Canonical Allele Identifier: CA359209863
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13776703A>G , CM000667.2:g.13776703A>G GRCh38
NC_000005.9:g.13776812A>G , CM000667.1:g.13776812A>G GRCh37
NC_000005.8:g.13829812A>G NCBI36
NG_013081.1:g.172778T>C
NG_013081.2:g.172778T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.9109T>C MANE Select ENSP00000265104.4:p.Ser3037Pro
ENST00000681290.1:c.9064T>C ENSP00000505288.1:p.Ser3022Pro
ENST00000265104.4:c.9109T>C ENSP00000265104.4:p.Ser3037Pro
NM_001369.2:c.9109T>C NP_001360.1:p.Ser3037Pro
XM_005248262.2:c.9064T>C XP_005248319.1:p.Ser3022Pro
XM_011513990.1:c.9104T>C XP_011512292.1:p.Leu3035Pro
XR_925598.1:n.9180T>C
XM_005248262.3:c.9217T>C XP_005248319.2:p.Ser3073Pro
XM_017009177.1:c.9217T>C XP_016864666.1:p.Ser3073Pro
XM_017009178.1:c.8122T>C XP_016864667.1:p.Ser2708Pro
XM_017009179.2:c.8122T>C XP_016864668.1:p.Ser2708Pro
XM_017009180.1:c.9217T>C XP_016864669.1:p.Ser3073Pro
XM_017009181.1:c.9217T>C XP_016864670.1:p.Ser3073Pro
XM_017009182.1:c.9217T>C XP_016864671.1:p.Ser3073Pro
XM_017009183.1:c.9217T>C XP_016864672.1:p.Ser3073Pro
XM_017009184.1:c.9212T>C XP_016864673.1:p.Leu3071Pro
XM_017009185.1:c.4306T>C XP_016864674.1:p.Ser1436Pro
XM_017009186.1:c.3859T>C XP_016864675.1:p.Ser1287Pro
XM_017009188.1:c.3196T>C XP_016864677.1:p.Ser1066Pro
XM_024454388.1:c.8122T>C XP_024310156.1:p.Ser2708Pro
XM_024454389.1:c.7711T>C XP_024310157.1:p.Ser2571Pro
XR_001742034.1:n.9103T>C
XR_001742035.1:n.9098T>C
NM_001369.3:c.9109T>C MANE Select NP_001360.1:p.Ser3037Pro