Canonical Allele Identifier: CA349933902

Gene: DNAH7

Linked Data

• gnomAD v4: 2-195787134-A-C
• MyVariant Identifiers: chr2:g.196651858A>C (hg19) ; chr2:g.195787134A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.195787134A>C , CM000664.2:g.195787134A>C	GRCh38
NC_000002.11:g.196651858A>C , CM000664.1:g.196651858A>C	GRCh37
NC_000002.10:g.196360103A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312428.11:c.10754T>G MANE Select	ENSP00000311273.6:p.Phe3585Cys
ENST00000312428.10:c.10754T>G	ENSP00000311273.6:p.Phe3585Cys
ENST00000409063.5:c.203T>G	ENSP00000386912.1:p.Phe68Cys
NM_018897.2:c.10754T>G	NP_061720.2:p.Phe3585Cys
XM_011511487.1:c.10754T>G	XP_011509789.1:p.Phe3585Cys
XM_011511488.1:c.10634T>G	XP_011509790.1:p.Phe3545Cys
XM_011511489.1:c.10616T>G	XP_011509791.1:p.Phe3539Cys
XM_011511490.1:c.10529T>G	XP_011509792.1:p.Phe3510Cys
XM_011511496.1:c.6398T>G	XP_011509798.1:p.Phe2133Cys
XM_011511497.1:c.5126T>G	XP_011509799.1:p.Phe1709Cys
XM_011511488.3:c.10634T>G	XP_011509790.1:p.Phe3545Cys
XM_011511489.2:c.10616T>G	XP_011509791.1:p.Phe3539Cys
XM_011511490.3:c.10529T>G	XP_011509792.1:p.Phe3510Cys
XM_011511497.2:c.5126T>G	XP_011509799.1:p.Phe1709Cys
XM_017004504.2:c.10481T>G	XP_016859993.1:p.Phe3494Cys
NM_018897.3:c.10754T>G MANE Select	NP_061720.2:p.Phe3585Cys