Canonical Allele Identifier: CA349933901
Gene: DNAH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.196651857A>T (hg19) chr2:g.195787133A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.195787133A>T , CM000664.2:g.195787133A>T GRCh38
NC_000002.11:g.196651857A>T , CM000664.1:g.196651857A>T GRCh37
NC_000002.10:g.196360102A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000312428.11:c.10755T>A MANE Select ENSP00000311273.6:p.Phe3585Leu
ENST00000312428.10:c.10755T>A ENSP00000311273.6:p.Phe3585Leu
ENST00000409063.5:c.204T>A ENSP00000386912.1:p.Phe68Leu
NM_018897.2:c.10755T>A NP_061720.2:p.Phe3585Leu
XM_011511487.1:c.10755T>A XP_011509789.1:p.Phe3585Leu
XM_011511488.1:c.10635T>A XP_011509790.1:p.Phe3545Leu
XM_011511489.1:c.10617T>A XP_011509791.1:p.Phe3539Leu
XM_011511490.1:c.10530T>A XP_011509792.1:p.Phe3510Leu
XM_011511496.1:c.6399T>A XP_011509798.1:p.Phe2133Leu
XM_011511497.1:c.5127T>A XP_011509799.1:p.Phe1709Leu
XM_011511488.3:c.10635T>A XP_011509790.1:p.Phe3545Leu
XM_011511489.2:c.10617T>A XP_011509791.1:p.Phe3539Leu
XM_011511490.3:c.10530T>A XP_011509792.1:p.Phe3510Leu
XM_011511497.2:c.5127T>A XP_011509799.1:p.Phe1709Leu
XM_017004504.2:c.10482T>A XP_016859993.1:p.Phe3494Leu
NM_018897.3:c.10755T>A MANE Select NP_061720.2:p.Phe3585Leu
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