Canonical Allele Identifier: CA8378088

Gene: MYH10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8577269A>G , CM000679.2:g.8577269A>G	GRCh38
NC_000017.10:g.8480587A>G , CM000679.1:g.8480587A>G	GRCh37
NC_000017.9:g.8421312A>G	NCBI36
NG_042305.1:g.58493T>C
NG_042305.2:g.58493T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411957.2:n.747T>C
ENST00000465458.2:n.799T>C
ENST00000684843.1:c.600T>C	ENSP00000509695.1:p.Ser200=
ENST00000685418.1:c.531-7457T>C	ENSP00000510761.1:n.531-7457T>C
ENST00000685884.1:n.1033T>C
ENST00000686521.1:n.843T>C
ENST00000686654.1:c.600T>C	ENSP00000508862.1:p.Ser200=
ENST00000686956.1:n.843T>C
ENST00000687178.1:c.600T>C	ENSP00000509748.1:p.Ser200=
ENST00000687661.1:n.747T>C
ENST00000688497.1:c.572T>C	ENSP00000509831.1:p.Leu191Pro
ENST00000688902.1:c.600T>C	ENSP00000509091.1:p.Ser200=
ENST00000690548.1:n.168T>C
ENST00000690895.1:n.747T>C
ENST00000691566.1:n.843T>C
ENST00000692077.1:n.843T>C
ENST00000692526.1:c.600T>C	ENSP00000510471.1:p.Ser200=
ENST00000692894.1:n.748T>C
ENST00000693441.1:c.600T>C	ENSP00000509241.1:p.Ser200=
ENST00000693704.1:n.747T>C
ENST00000360416.8:c.600T>C MANE Select	ENSP00000353590.4:p.Ser200=
ENST00000269243.8:c.600T>C	ENSP00000269243.4:p.Ser200=
ENST00000360416.7:c.600T>C	ENSP00000353590.3:p.Ser200=
ENST00000379980.8:c.600T>C	ENSP00000369315.5:p.Ser200=
ENST00000472728.1:n.166T>C
NM_001256012.1:c.600T>C	NP_001242941.1:p.Ser200=
NM_001256095.1:c.600T>C	NP_001243024.1:p.Ser200=
NM_005964.3:c.600T>C	NP_005955.3:p.Ser200=
XM_005256651.2:c.600T>C	XP_005256708.1:p.Ser200=
XM_011523875.1:c.690T>C	XP_011522177.1:p.Ser230=
XM_011523876.1:c.690T>C	XP_011522178.1:p.Ser230=
XM_011523877.1:c.690T>C	XP_011522179.1:p.Ser230=
XM_011523878.1:c.690T>C	XP_011522180.1:p.Ser230=
XM_011523879.1:c.690T>C	XP_011522181.1:p.Ser230=
XM_011523880.1:c.690T>C	XP_011522182.1:p.Ser230=
XM_011523875.2:c.690T>C	XP_011522177.1:p.Ser230=
XM_011523878.2:c.690T>C	XP_011522180.1:p.Ser230=
XM_011523879.2:c.690T>C	XP_011522181.1:p.Ser230=
XM_011523880.2:c.690T>C	XP_011522182.1:p.Ser230=
XM_017024677.2:c.600T>C	XP_016880166.1:p.Ser200=
XM_017024678.1:c.600T>C	XP_016880167.1:p.Ser200=
XM_017024679.1:c.600T>C	XP_016880168.1:p.Ser200=
XM_017024680.1:c.600T>C	XP_016880169.1:p.Ser200=
XM_017024681.1:c.600T>C	XP_016880170.1:p.Ser200=
XM_017024682.1:c.600T>C	XP_016880171.1:p.Ser200=
NM_001256012.3:c.600T>C MANE Select	NP_001242941.1:p.Ser200=
NM_001375266.1:c.600T>C	NP_001362195.1:p.Ser200=
NM_005964.4:c.600T>C	NP_005955.3:p.Ser200=
NM_001256095.2:c.600T>C	NP_001243024.1:p.Ser200=
NM_005964.5:c.600T>C	NP_005955.3:p.Ser200=