Canonical Allele Identifier: CA3202142
Community Standard Title: NM_001369.3(DNAH5):c.10774A>C (p.Ile3592Leu)
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13753331T>G , CM000667.2:g.13753331T>G GRCh38
NC_000005.9:g.13753440T>G , CM000667.1:g.13753440T>G GRCh37
NC_000005.8:g.13806440T>G NCBI36
NG_013081.1:g.196150A>C
NG_013081.2:g.196150A>C

Transcript Alleles

HGVS Amino-acid Change
NM_001369.3:c.10774A>C MANE Select NP_001360.1:p.Ile3592Leu
ENST00000265104.5:c.10774A>C MANE Select ENSP00000265104.4:p.Ile3592Leu
NM_001369.2:c.10774A>C NP_001360.1:p.Ile3592Leu
ENST00000265104.4:c.10774A>C ENSP00000265104.4:p.Ile3592Leu
ENST00000681290.1:c.10729A>C ENSP00000505288.1:p.Ile3577Leu
XM_005248262.2:c.10729A>C XP_005248319.1:p.Ile3577Leu
XM_005248262.3:c.10882A>C XP_005248319.2:p.Ile3628Leu
XM_017009177.1:c.10882A>C XP_016864666.1:p.Ile3628Leu
XM_017009178.1:c.9787A>C XP_016864667.1:p.Ile3263Leu
XM_017009179.2:c.9787A>C XP_016864668.1:p.Ile3263Leu
XM_017009180.1:c.10882A>C XP_016864669.1:p.Ile3628Leu
XM_017009181.1:c.10882A>C XP_016864670.1:p.Ile3628Leu
XM_017009182.1:c.10882A>C XP_016864671.1:p.Ile3628Leu
XM_017009185.1:c.5971A>C XP_016864674.1:p.Ile1991Leu
XM_017009186.1:c.5524A>C XP_016864675.1:p.Ile1842Leu
XM_017009188.1:c.4861A>C XP_016864677.1:p.Ile1621Leu
XM_024454388.1:c.9787A>C XP_024310156.1:p.Ile3263Leu
XM_024454389.1:c.9376A>C XP_024310157.1:p.Ile3126Leu