Canonical Allele Identifier: CA113979098
Community Standard Title: NM_001369.3(DNAH5):c.7571C>T (p.Pro2524Leu)
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13810097G>A , CM000667.2:g.13810097G>A GRCh38
NC_000005.9:g.13810206G>A , CM000667.1:g.13810206G>A GRCh37
NC_000005.8:g.13863206G>A NCBI36
NG_013081.1:g.139384C>T
NG_013081.2:g.139384C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001369.3:c.7571C>T MANE Select NP_001360.1:p.Pro2524Leu
ENST00000265104.5:c.7571C>T MANE Select ENSP00000265104.4:p.Pro2524Leu
NM_001369.2:c.7571C>T NP_001360.1:p.Pro2524Leu
ENST00000265104.4:c.7571C>T ENSP00000265104.4:p.Pro2524Leu
ENST00000512443.1:n.427C>T
ENST00000681290.1:c.7526C>T ENSP00000505288.1:p.Pro2509Leu
XM_005248262.2:c.7526C>T XP_005248319.1:p.Pro2509Leu
XM_005248262.3:c.7679C>T XP_005248319.2:p.Pro2560Leu
XM_011513990.1:c.7571C>T XP_011512292.1:p.Pro2524Leu
XM_017009177.1:c.7679C>T XP_016864666.1:p.Pro2560Leu
XM_017009178.1:c.6584C>T XP_016864667.1:p.Pro2195Leu
XM_017009179.2:c.6584C>T XP_016864668.1:p.Pro2195Leu
XM_017009180.1:c.7679C>T XP_016864669.1:p.Pro2560Leu
XM_017009181.1:c.7679C>T XP_016864670.1:p.Pro2560Leu
XM_017009182.1:c.7679C>T XP_016864671.1:p.Pro2560Leu
XM_017009183.1:c.7679C>T XP_016864672.1:p.Pro2560Leu
XM_017009184.1:c.7679C>T XP_016864673.1:p.Pro2560Leu
XM_017009185.1:c.2768C>T XP_016864674.1:p.Pro923Leu
XM_017009186.1:c.2321C>T XP_016864675.1:p.Pro774Leu
XM_017009187.1:c.7679C>T XP_016864676.1:p.Pro2560Leu
XM_017009188.1:c.1658C>T XP_016864677.1:p.Pro553Leu
XM_024454388.1:c.6584C>T XP_024310156.1:p.Pro2195Leu
XM_024454389.1:c.6173C>T XP_024310157.1:p.Pro2058Leu
XR_001742034.1:n.7696C>T
XR_001742035.1:n.7696C>T
XR_925598.1:n.7778C>T