Canonical Allele Identifier: CA287620402

Gene: MYH10 NDEL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8478363C>T , CM000679.2:g.8478363C>T	GRCh38
NC_000017.10:g.8381681C>T , CM000679.1:g.8381681C>T	GRCh37
NC_000017.9:g.8322406C>T	NCBI36
NG_042305.1:g.157399G>A
NG_042305.2:g.157399G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684843.1:c.5618G>A (MYH10)	ENSP00000509695.1:p.Arg1873Gln
ENST00000685418.1:c.*4885G>A (MYH10)	ENSP00000510761.1:n.*4885G>A
ENST00000685631.1:n.6586G>A (MYH10)
ENST00000686521.1:n.5924G>A (MYH10)
ENST00000686654.1:c.5681G>A (MYH10)	ENSP00000508862.1:p.Arg1894Gln
ENST00000687178.1:c.5615G>A (MYH10)	ENSP00000509748.1:p.Arg1872Gln
ENST00000688497.1:c.*4963G>A (MYH10)	ENSP00000509831.1:n.*4963G>A
ENST00000688902.1:c.5681G>A (MYH10)	ENSP00000509091.1:p.Arg1894Gln
ENST00000691566.1:n.8651G>A (MYH10)
ENST00000692526.1:c.5618G>A (MYH10)	ENSP00000510471.1:p.Arg1873Gln
ENST00000693441.1:c.5681G>A (MYH10)	ENSP00000509241.1:p.Arg1894Gln
ENST00000360416.8:c.5681G>A (MYH10) MANE Select	ENSP00000353590.4:p.Arg1894Gln
ENST00000269243.8:c.5588G>A (MYH10)	ENSP00000269243.4:p.Arg1863Gln
ENST00000360416.7:c.5681G>A (MYH10)	ENSP00000353590.3:p.Arg1894Gln
ENST00000379980.8:c.5615G>A (MYH10)	ENSP00000369315.5:p.Arg1872Gln
ENST00000476737.1:n.541G>A (MYH10)
ENST00000581679.1:c.418-11884C>T (NDEL1)
NM_001256012.1:c.5681G>A (MYH10)	NP_001242941.1:p.Arg1894Gln
NM_001256095.1:c.5615G>A (MYH10)	NP_001243024.1:p.Arg1872Gln
NM_005964.3:c.5588G>A (MYH10)	NP_005955.3:p.Arg1863Gln
XM_005256651.2:c.5681G>A (MYH10)	XP_005256708.1:p.Arg1894Gln
XM_011523875.1:c.5771G>A (MYH10)	XP_011522177.1:p.Arg1924Gln
XM_011523876.1:c.5768G>A (MYH10)	XP_011522178.1:p.Arg1923Gln
XM_011523877.1:c.5741G>A (MYH10)	XP_011522179.1:p.Arg1914Gln
XM_011523878.1:c.5708G>A (MYH10)	XP_011522180.1:p.Arg1903Gln
XM_011523879.1:c.5705G>A (MYH10)	XP_011522181.1:p.Arg1902Gln
XM_011523880.1:c.5678G>A (MYH10)	XP_011522182.1:p.Arg1893Gln
XM_011523875.2:c.5771G>A (MYH10)	XP_011522177.1:p.Arg1924Gln
XM_011523878.2:c.5708G>A (MYH10)	XP_011522180.1:p.Arg1903Gln
XM_011523879.2:c.5705G>A (MYH10)	XP_011522181.1:p.Arg1902Gln
XM_011523880.2:c.5678G>A (MYH10)	XP_011522182.1:p.Arg1893Gln
XM_017024677.2:c.5618G>A (MYH10)	XP_016880166.1:p.Arg1873Gln
XM_017024678.1:c.5618G>A (MYH10)	XP_016880167.1:p.Arg1873Gln
XM_017024679.1:c.5618G>A (MYH10)	XP_016880168.1:p.Arg1873Gln
XM_017024680.1:c.5615G>A (MYH10)	XP_016880169.1:p.Arg1872Gln
XM_017024681.1:c.5588G>A (MYH10)	XP_016880170.1:p.Arg1863Gln
XM_017024682.1:c.5588G>A (MYH10)	XP_016880171.1:p.Arg1863Gln
NM_001256012.3:c.5681G>A (MYH10) MANE Select	NP_001242941.1:p.Arg1894Gln
NM_001375266.1:c.5618G>A (MYH10)	NP_001362195.1:p.Arg1873Gln
NM_005964.4:c.5588G>A (MYH10)	NP_005955.3:p.Arg1863Gln
NM_001256095.2:c.5615G>A (MYH10)	NP_001243024.1:p.Arg1872Gln
NM_005964.5:c.5588G>A (MYH10)	NP_005955.3:p.Arg1863Gln