Canonical Allele Identifier: CA398028525

Gene: MYH10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8490479A>G , CM000679.2:g.8490479A>G	GRCh38
NC_000017.10:g.8393797A>G , CM000679.1:g.8393797A>G	GRCh37
NC_000017.9:g.8334522A>G	NCBI36
NG_042305.1:g.145283T>C
NG_042305.2:g.145283T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684843.1:c.4682T>C	ENSP00000509695.1:p.Leu1561Pro
ENST00000685418.1:c.*3949T>C	ENSP00000510761.1:n.*3949T>C
ENST00000686521.1:n.4988T>C
ENST00000686654.1:c.4745T>C	ENSP00000508862.1:p.Leu1582Pro
ENST00000687178.1:c.4679T>C	ENSP00000509748.1:p.Leu1560Pro
ENST00000688497.1:c.*4027T>C	ENSP00000509831.1:n.*4027T>C
ENST00000688902.1:c.4745T>C	ENSP00000509091.1:p.Leu1582Pro
ENST00000691566.1:n.4988T>C
ENST00000692077.1:n.4988T>C
ENST00000692526.1:c.4682T>C	ENSP00000510471.1:p.Leu1561Pro
ENST00000693441.1:c.4745T>C	ENSP00000509241.1:p.Leu1582Pro
ENST00000360416.8:c.4745T>C MANE Select	ENSP00000353590.4:p.Leu1582Pro
ENST00000269243.8:c.4652T>C	ENSP00000269243.4:p.Leu1551Pro
ENST00000360416.7:c.4745T>C	ENSP00000353590.3:p.Leu1582Pro
ENST00000379980.8:c.4679T>C	ENSP00000369315.5:p.Leu1560Pro
NM_001256012.1:c.4745T>C	NP_001242941.1:p.Leu1582Pro
NM_001256095.1:c.4679T>C	NP_001243024.1:p.Leu1560Pro
NM_005964.3:c.4652T>C	NP_005955.3:p.Leu1551Pro
XM_005256651.2:c.4745T>C	XP_005256708.1:p.Leu1582Pro
XM_011523875.1:c.4835T>C	XP_011522177.1:p.Leu1612Pro
XM_011523876.1:c.4832T>C	XP_011522178.1:p.Leu1611Pro
XM_011523877.1:c.4805T>C	XP_011522179.1:p.Leu1602Pro
XM_011523878.1:c.4772T>C	XP_011522180.1:p.Leu1591Pro
XM_011523879.1:c.4769T>C	XP_011522181.1:p.Leu1590Pro
XM_011523880.1:c.4742T>C	XP_011522182.1:p.Leu1581Pro
XM_011523875.2:c.4835T>C	XP_011522177.1:p.Leu1612Pro
XM_011523878.2:c.4772T>C	XP_011522180.1:p.Leu1591Pro
XM_011523879.2:c.4769T>C	XP_011522181.1:p.Leu1590Pro
XM_011523880.2:c.4742T>C	XP_011522182.1:p.Leu1581Pro
XM_017024677.2:c.4682T>C	XP_016880166.1:p.Leu1561Pro
XM_017024678.1:c.4682T>C	XP_016880167.1:p.Leu1561Pro
XM_017024679.1:c.4682T>C	XP_016880168.1:p.Leu1561Pro
XM_017024680.1:c.4679T>C	XP_016880169.1:p.Leu1560Pro
XM_017024681.1:c.4652T>C	XP_016880170.1:p.Leu1551Pro
XM_017024682.1:c.4652T>C	XP_016880171.1:p.Leu1551Pro
NM_001256012.3:c.4745T>C MANE Select	NP_001242941.1:p.Leu1582Pro
NM_001375266.1:c.4682T>C	NP_001362195.1:p.Leu1561Pro
NM_005964.4:c.4652T>C	NP_005955.3:p.Leu1551Pro
NM_001256095.2:c.4679T>C	NP_001243024.1:p.Leu1560Pro
NM_005964.5:c.4652T>C	NP_005955.3:p.Leu1551Pro