Canonical Allele Identifier: CA235282

Gene: MYH10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8513561C>A , CM000679.2:g.8513561C>A	GRCh38
NC_000017.10:g.8416879C>A , CM000679.1:g.8416879C>A	GRCh37
NC_000017.9:g.8357604C>A	NCBI36
NG_042305.1:g.122201G>T
NG_042305.2:g.122201G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465458.2:n.2858G>T
ENST00000684843.1:c.2659G>T	ENSP00000509695.1:p.Glu887Ter
ENST00000685418.1:c.*1926G>T	ENSP00000510761.1:n.*1926G>T
ENST00000686521.1:n.2965G>T
ENST00000686654.1:c.2722G>T	ENSP00000508862.1:p.Glu908Ter
ENST00000686956.1:n.2965G>T
ENST00000687178.1:c.2656G>T	ENSP00000509748.1:p.Glu886Ter
ENST00000688497.1:c.*2004G>T	ENSP00000509831.1:n.*2004G>T
ENST00000688902.1:c.2722G>T	ENSP00000509091.1:p.Glu908Ter
ENST00000691566.1:n.2965G>T
ENST00000692077.1:n.2965G>T
ENST00000692526.1:c.2659G>T	ENSP00000510471.1:p.Glu887Ter
ENST00000693441.1:c.2722G>T	ENSP00000509241.1:p.Glu908Ter
ENST00000360416.8:c.2722G>T MANE Select	ENSP00000353590.4:p.Glu908Ter
ENST00000269243.8:c.2629G>T	ENSP00000269243.4:p.Glu877Ter
ENST00000360416.7:c.2722G>T	ENSP00000353590.3:p.Glu908Ter
ENST00000379980.8:c.2656G>T	ENSP00000369315.5:p.Glu886Ter
NM_001256012.1:c.2722G>T	NP_001242941.1:p.Glu908Ter
NM_001256095.1:c.2656G>T	NP_001243024.1:p.Glu886Ter
NM_005964.3:c.2629G>T	NP_005955.3:p.Glu877Ter
XM_005256651.2:c.2722G>T	XP_005256708.1:p.Glu908Ter
XM_011523875.1:c.2812G>T	XP_011522177.1:p.Glu938Ter
XM_011523876.1:c.2809G>T	XP_011522178.1:p.Glu937Ter
XM_011523877.1:c.2782G>T	XP_011522179.1:p.Glu928Ter
XM_011523878.1:c.2749G>T	XP_011522180.1:p.Glu917Ter
XM_011523879.1:c.2746G>T	XP_011522181.1:p.Glu916Ter
XM_011523880.1:c.2719G>T	XP_011522182.1:p.Glu907Ter
XR_934209.1:n.493-151C>A
XR_934210.1:n.1074-151C>A
XR_934211.1:n.736-151C>A
XM_011523875.2:c.2812G>T	XP_011522177.1:p.Glu938Ter
XM_011523878.2:c.2749G>T	XP_011522180.1:p.Glu917Ter
XM_011523879.2:c.2746G>T	XP_011522181.1:p.Glu916Ter
XM_011523880.2:c.2719G>T	XP_011522182.1:p.Glu907Ter
XM_017024677.2:c.2659G>T	XP_016880166.1:p.Glu887Ter
XM_017024678.1:c.2659G>T	XP_016880167.1:p.Glu887Ter
XM_017024679.1:c.2659G>T	XP_016880168.1:p.Glu887Ter
XM_017024680.1:c.2656G>T	XP_016880169.1:p.Glu886Ter
XM_017024681.1:c.2629G>T	XP_016880170.1:p.Glu877Ter
XM_017024682.1:c.2629G>T	XP_016880171.1:p.Glu877Ter
XR_001752779.1:n.704-151C>A
XR_934210.2:n.796-151C>A
XR_934211.2:n.458-151C>A
NM_001256012.3:c.2722G>T MANE Select	NP_001242941.1:p.Glu908Ter
NM_001375266.1:c.2659G>T	NP_001362195.1:p.Glu887Ter
NM_005964.4:c.2629G>T	NP_005955.3:p.Glu877Ter
NM_001256095.2:c.2656G>T	NP_001243024.1:p.Glu886Ter
NM_005964.5:c.2629G>T	NP_005955.3:p.Glu877Ter