Canonical Allele Identifier: CA8376624

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8475843G>A , CM000679.2:g.8475843G>A GRCh38
NC_000017.10:g.8379161G>A , CM000679.1:g.8379161G>A GRCh37
NC_000017.9:g.8319886G>A NCBI36
NG_042305.1:g.159919C>T
NG_042305.2:g.159919C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684843.1:c.5922C>T (MYH10) ENSP00000509695.1:p.Thr1974=
ENST00000685418.1:c.*5189C>T (MYH10) ENSP00000510761.1:n.*5189C>T
ENST00000685631.1:n.6890C>T (MYH10)
ENST00000686521.1:n.7517C>T (MYH10)
ENST00000686654.1:c.5985C>T (MYH10) ENSP00000508862.1:p.Thr1995=
ENST00000687178.1:c.5919C>T (MYH10) ENSP00000509748.1:p.Thr1973=
ENST00000688497.1:c.*5267C>T (MYH10) ENSP00000509831.1:n.*5267C>T
ENST00000688902.1:c.5985C>T (MYH10) ENSP00000509091.1:p.Thr1995=
ENST00000691566.1:n.8955C>T (MYH10)
ENST00000692526.1:c.5922C>T (MYH10) ENSP00000510471.1:p.Thr1974=
ENST00000693441.1:c.5985C>T (MYH10) ENSP00000509241.1:p.Thr1995=
ENST00000360416.8:c.5985C>T (MYH10) MANE Select ENSP00000353590.4:p.Thr1995=
ENST00000269243.8:c.5892C>T (MYH10) ENSP00000269243.4:p.Thr1964=
ENST00000360416.7:c.5985C>T (MYH10) ENSP00000353590.3:p.Thr1995=
ENST00000379980.8:c.5919C>T (MYH10) ENSP00000369315.5:p.Thr1973=
ENST00000581679.1:c.418-14404G>A (NDEL1)
NM_001256012.1:c.5985C>T (MYH10) NP_001242941.1:p.Thr1995=
NM_001256095.1:c.5919C>T (MYH10) NP_001243024.1:p.Thr1973=
NM_005964.3:c.5892C>T (MYH10) NP_005955.3:p.Thr1964=
XM_005256651.2:c.5985C>T (MYH10) XP_005256708.1:p.Thr1995=
XM_011523875.1:c.6075C>T (MYH10) XP_011522177.1:p.Thr2025=
XM_011523876.1:c.6072C>T (MYH10) XP_011522178.1:p.Thr2024=
XM_011523877.1:c.6045C>T (MYH10) XP_011522179.1:p.Thr2015=
XM_011523878.1:c.6012C>T (MYH10) XP_011522180.1:p.Thr2004=
XM_011523879.1:c.6009C>T (MYH10) XP_011522181.1:p.Thr2003=
XM_011523880.1:c.5982C>T (MYH10) XP_011522182.1:p.Thr1994=
XM_011523875.2:c.6075C>T (MYH10) XP_011522177.1:p.Thr2025=
XM_011523878.2:c.6012C>T (MYH10) XP_011522180.1:p.Thr2004=
XM_011523879.2:c.6009C>T (MYH10) XP_011522181.1:p.Thr2003=
XM_011523880.2:c.5982C>T (MYH10) XP_011522182.1:p.Thr1994=
XM_017024677.2:c.5922C>T (MYH10) XP_016880166.1:p.Thr1974=
XM_017024678.1:c.5922C>T (MYH10) XP_016880167.1:p.Thr1974=
XM_017024679.1:c.5922C>T (MYH10) XP_016880168.1:p.Thr1974=
XM_017024680.1:c.5919C>T (MYH10) XP_016880169.1:p.Thr1973=
XM_017024681.1:c.5892C>T (MYH10) XP_016880170.1:p.Thr1964=
XM_017024682.1:c.5892C>T (MYH10) XP_016880171.1:p.Thr1964=
NM_001256012.3:c.5985C>T (MYH10) MANE Select NP_001242941.1:p.Thr1995=
NM_001375266.1:c.5922C>T (MYH10) NP_001362195.1:p.Thr1974=
NM_005964.4:c.5892C>T (MYH10) NP_005955.3:p.Thr1964=
NM_001256095.2:c.5919C>T (MYH10) NP_001243024.1:p.Thr1973=
NM_005964.5:c.5892C>T (MYH10) NP_005955.3:p.Thr1964=