Canonical Allele Identifier: CA2806025212

Gene: MYH11 NDE1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.15715085_15715166del , CM000678.2:g.15715085_15715166del	GRCh38
NC_000016.9:g.15808942_15809023del , CM000678.1:g.15808942_15809023del	GRCh37
NC_000016.8:g.15716443_15716524del	NCBI36
NG_009299.1:g.146869_146950del
NG_021210.1:g.76819_76900del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300036.6:c.5613+2_5614del (MYH11)
ENST00000396354.6:c.948-9106_948-9025del (NDE1) MANE Select	ENSP00000379642.1:n.948-9106_948-9025del
ENST00000452625.7:c.5634+2_5635del (MYH11)
ENST00000572756.6:c.796-9106_796-9025del (NDE1)	ENSP00000460436.2:n.796-9106_796-9025del
ENST00000576164.6:n.3533+2_3534del (MYH11)
ENST00000576790.7:c.5613+2_5614del (MYH11)
ENST00000577101.6:c.1031-9106_1031-9025del (NDE1)	ENSP00000461729.2:n.1031-9106_1031-9025del
ENST00000652121.1:c.*3796+2_*3797del (MYH11)
ENST00000674538.1:c.796-9106_796-9025del (NDE1)	ENSP00000501547.1:n.796-9106_796-9025del
ENST00000674554.1:c.948-9106_948-9025del (NDE1)	ENSP00000502635.1:n.948-9106_948-9025del
ENST00000674581.1:c.*7-9106_*7-9025del (NDE1)	ENSP00000502100.1:n.*7-9106_*7-9025del
ENST00000674588.1:c.796-9106_796-9025del (NDE1)	ENSP00000502802.1:n.796-9106_796-9025del
ENST00000674888.1:c.948-9106_948-9025del (NDE1)	ENSP00000501936.1:n.948-9106_948-9025del
ENST00000674900.1:c.*349-9106_*349-9025del (NDE1)	ENSP00000502662.1:n.*349-9106_*349-9025del
ENST00000674995.1:c.796-9190_796-9109del (NDE1)	ENSP00000502414.1:n.796-9190_796-9109del
ENST00000675171.1:c.*700-9106_*700-9025del (NDE1)	ENSP00000501812.1:n.*700-9106_*700-9025del
ENST00000675926.1:c.948-9106_948-9025del (NDE1)	ENSP00000502354.1:n.948-9106_948-9025del
ENST00000675951.1:c.948-9106_948-9025del (NDE1)	ENSP00000502160.1:n.948-9106_948-9025del
ENST00000300036.5:c.5613+2_5614del (MYH11)
ENST00000342673.9:c.948-9106_948-9025del (NDE1)	ENSP00000345892.5:n.948-9106_948-9025del
ENST00000396324.7:c.5634+2_5635del (MYH11)
ENST00000396354.5:c.948-9106_948-9025del (NDE1)	ENSP00000379642.1:n.948-9106_948-9025del
ENST00000396355.5:c.948-9106_948-9025del (NDE1)	ENSP00000379643.1:n.948-9106_948-9025del
ENST00000452625.6:c.5634+2_5635del (MYH11)
ENST00000571275.1:n.1901+2_1902del (MYH11)
ENST00000572967.1:c.453-9106_453-9025del (NDE1)	ENSP00000459918.1:n.453-9106_453-9025del
ENST00000573694.5:c.380-9106_380-9025del (NDE1)
ENST00000576164.5:n.3533+2_3534del (MYH11)
ENST00000576790.6:c.5613+2_5614del (MYH11)
ENST00000616439.4:c.5634+2_5635del (MYH11)
NM_001040113.1:c.5634+2_5635del (MYH11)
NM_001040114.1:c.5634+2_5635del (MYH11)
NM_001143979.1:c.948-9106_948-9025del (NDE1)	NP_001137451.1:n.948-9106_948-9025del
NM_002474.2:c.5613+2_5614del (MYH11)
NM_017668.2:c.948-9106_948-9025del (NDE1)	NP_060138.1:n.948-9106_948-9025del
NM_022844.2:c.5613+2_5614del (MYH11)
XM_011522502.1:c.5613+2_5614del (MYH11)
XM_011522502.2:c.5613+2_5614del (MYH11)
XM_017023250.1:c.5634+2_5635del (MYH11)
NM_002474.3:c.5613+2_5614del (MYH11)
NM_017668.3:c.948-9106_948-9025del (NDE1) MANE Select	NP_060138.1:n.948-9106_948-9025del
NM_001040113.2:c.5634+2_5635del (MYH11)
NM_001143979.2:c.948-9106_948-9025del (NDE1)	NP_001137451.1:n.948-9106_948-9025del
NM_001040114.2:c.5634+2_5635del (MYH11)
NM_022844.3:c.5613+2_5614del (MYH11)