Canonical Allele Identifier: CA2209922881

Linked Data

dbSNP Id: rs2040062858

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.15715271_15715274del , CM000678.2:g.15715271_15715274del GRCh38
NC_000016.9:g.15809128_15809131del , CM000678.1:g.15809128_15809131del GRCh37
NC_000016.8:g.15716629_15716632del NCBI36
NG_009299.1:g.146760_146763del
NG_021210.1:g.77005_77008del

Transcript Alleles

HGVS Amino-acid Change
ENST00000300036.6:c.5506_5509del (MYH11)
ENST00000396354.6:c.948-8920_948-8917del (NDE1) MANE Select ENSP00000379642.1:n.948-8920_948-8917del
ENST00000452625.7:c.5527_5530del (MYH11)
ENST00000572756.6:c.796-8920_796-8917del (NDE1) ENSP00000460436.2:n.796-8920_796-8917del
ENST00000576164.6:n.3426_3429del (MYH11)
ENST00000576790.7:c.5506_5509del (MYH11)
ENST00000577101.6:c.1031-8920_1031-8917del (NDE1) ENSP00000461729.2:n.1031-8920_1031-8917del
ENST00000652121.1:c.*3689_*3692del (MYH11)
ENST00000674538.1:c.796-8920_796-8917del (NDE1) ENSP00000501547.1:n.796-8920_796-8917del
ENST00000674554.1:c.948-8920_948-8917del (NDE1) ENSP00000502635.1:n.948-8920_948-8917del
ENST00000674581.1:c.*7-8920_*7-8917del (NDE1) ENSP00000502100.1:n.*7-8920_*7-8917del
ENST00000674588.1:c.796-8920_796-8917del (NDE1) ENSP00000502802.1:n.796-8920_796-8917del
ENST00000674888.1:c.948-8920_948-8917del (NDE1) ENSP00000501936.1:n.948-8920_948-8917del
ENST00000674900.1:c.*349-8920_*349-8917del (NDE1) ENSP00000502662.1:n.*349-8920_*349-8917del
ENST00000674995.1:c.796-9004_796-9001del (NDE1) ENSP00000502414.1:n.796-9004_796-9001del
ENST00000675171.1:c.*700-8920_*700-8917del (NDE1) ENSP00000501812.1:n.*700-8920_*700-8917del
ENST00000675926.1:c.948-8920_948-8917del (NDE1) ENSP00000502354.1:n.948-8920_948-8917del
ENST00000675951.1:c.948-8920_948-8917del (NDE1) ENSP00000502160.1:n.948-8920_948-8917del
ENST00000300036.5:c.5506_5509del (MYH11)
ENST00000342673.9:c.948-8920_948-8917del (NDE1) ENSP00000345892.5:n.948-8920_948-8917del
ENST00000396324.7:c.5527_5530del (MYH11)
ENST00000396354.5:c.948-8920_948-8917del (NDE1) ENSP00000379642.1:n.948-8920_948-8917del
ENST00000396355.5:c.948-8920_948-8917del (NDE1) ENSP00000379643.1:n.948-8920_948-8917del
ENST00000452625.6:c.5527_5530del (MYH11)
ENST00000571275.1:n.1794_1797del (MYH11)
ENST00000572967.1:c.453-8920_453-8917del (NDE1) ENSP00000459918.1:n.453-8920_453-8917del
ENST00000573694.5:c.380-8920_380-8917del (NDE1)
ENST00000576164.5:n.3426_3429del (MYH11)
ENST00000576790.6:c.5506_5509del (MYH11)
ENST00000616439.4:c.5527_5530del (MYH11)
NM_001040113.1:c.5527_5530del (MYH11)
NM_001040114.1:c.5527_5530del (MYH11)
NM_001143979.1:c.948-8920_948-8917del (NDE1) NP_001137451.1:n.948-8920_948-8917del
NM_002474.2:c.5506_5509del (MYH11)
NM_017668.2:c.948-8920_948-8917del (NDE1) NP_060138.1:n.948-8920_948-8917del
NM_022844.2:c.5506_5509del (MYH11)
XM_011522502.1:c.5506_5509del (MYH11)
XM_011522502.2:c.5506_5509del (MYH11)
XM_017023250.1:c.5527_5530del (MYH11)
NM_002474.3:c.5506_5509del (MYH11)
NM_017668.3:c.948-8920_948-8917del (NDE1) MANE Select NP_060138.1:n.948-8920_948-8917del
NM_001040113.2:c.5527_5530del (MYH11)
NM_001143979.2:c.948-8920_948-8917del (NDE1) NP_001137451.1:n.948-8920_948-8917del
NM_001040114.2:c.5527_5530del (MYH11)
NM_022844.3:c.5506_5509del (MYH11)