Canonical Allele Identifier: CA306461

Gene: MYH11 NDE1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.15724639del , CM000678.2:g.15724639del	GRCh38
NC_000016.9:g.15818496del , CM000678.1:g.15818496del	GRCh37
NC_000016.8:g.15725997del	NCBI36
NG_009299.1:g.137395del
NG_021210.1:g.86373del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300036.6:c.4116+11del (MYH11) MANE Select	ENSP00000300036.5:n.4116+11del
ENST00000396354.6:c.*388del (NDE1) MANE Select	ENSP00000379642.1:n.*388del
ENST00000452625.7:c.4137+11del (MYH11) MANE Plus Clinical	ENSP00000407821.2:n.4137+11del
ENST00000576790.7:c.4116+11del (MYH11)	ENSP00000458731.1:n.4116+11del
ENST00000577101.6:c.1479del (NDE1)	ENSP00000461729.2:n.1479del
ENST00000652121.1:c.*2299+11del (MYH11)	ENSP00000498314.1:n.*2299+11del
ENST00000674538.1:c.*206del (NDE1)	ENSP00000501547.1:n.*206del
ENST00000674554.1:c.*388del (NDE1)	ENSP00000502635.1:n.*388del
ENST00000674581.1:c.*455del (NDE1)	ENSP00000502100.1:n.*455del
ENST00000674588.1:c.*206del (NDE1)	ENSP00000502802.1:n.*206del
ENST00000674888.1:c.*388del (NDE1)	ENSP00000501936.1:n.*388del
ENST00000674900.1:c.*797del (NDE1)	ENSP00000502662.1:n.*797del
ENST00000674995.1:c.*206del (NDE1)	ENSP00000502414.1:n.*206del
ENST00000675171.1:c.*1148del (NDE1)	ENSP00000501812.1:n.*1148del
ENST00000675926.1:c.*388del (NDE1)	ENSP00000502354.1:n.*388del
ENST00000675951.1:c.*388del (NDE1)	ENSP00000502160.1:n.*388del
ENST00000300036.5:c.4116+11del (MYH11)	ENSP00000300036.5:n.4116+11del
ENST00000342673.9:c.*388del (NDE1)	ENSP00000345892.5:n.*388del
ENST00000396324.7:c.4137+11del (MYH11)	ENSP00000379616.3:n.4137+11del
ENST00000396354.5:c.*388del (NDE1)	ENSP00000379642.1:n.*388del
ENST00000396355.5:c.*388del (NDE1)	ENSP00000379643.1:n.*388del
ENST00000452625.6:c.4137+11del (MYH11)	ENSP00000407821.2:n.4137+11del
ENST00000571275.1:n.404+11del (MYH11)
ENST00000576790.6:c.4116+11del (MYH11)	ENSP00000458731.1:n.4116+11del
ENST00000616439.4:c.4137+11del (MYH11)	ENSP00000484924.1:n.4137+11del
NM_001040113.1:c.4137+11del (MYH11)	NP_001035202.1:n.4137+11del
NM_001040114.1:c.4137+11del (MYH11)	NP_001035203.1:n.4137+11del
NM_001143979.1:c.*388del (NDE1)	NP_001137451.1:n.*388del
NM_002474.2:c.4116+11del (MYH11)	NP_002465.1:n.4116+11del
NM_017668.2:c.*388del (NDE1)	NP_060138.1:n.*388del
NM_022844.2:c.4116+11del (MYH11)	NP_074035.1:n.4116+11del
XM_011522502.1:c.4116+11del (MYH11)	XP_011520804.1:n.4116+11del
XM_011522502.2:c.4116+11del (MYH11)	XP_011520804.1:n.4116+11del
XM_017023250.1:c.4137+11del (MYH11)	XP_016878739.1:n.4137+11del
NM_002474.3:c.4116+11del (MYH11) MANE Select	NP_002465.1:n.4116+11del
NM_017668.3:c.*388del (NDE1) MANE Select	NP_060138.1:n.*388del
NM_001040113.2:c.4137+11del (MYH11) MANE Plus Clinical	NP_001035202.1:n.4137+11del
NM_001143979.2:c.*388del (NDE1)	NP_001137451.1:n.*388del
NM_001040114.2:c.4137+11del (MYH11)	NP_001035203.1:n.4137+11del
NM_022844.3:c.4116+11del (MYH11)	NP_074035.1:n.4116+11del