Canonical Allele Identifier: CA377103733

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68121601G>A , CM000672.2:g.68121601G>A	GRCh38
NC_000010.10:g.69881358G>A , CM000672.1:g.69881358G>A	GRCh37
NC_000010.9:g.69551364G>A	NCBI36
NG_032118.1:g.20485G>A , LRG_410:g.20485G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.77+14800G>A	ENSP00000346369.2:n.77+14800G>A
ENST00000373675.4:c.163G>A	ENSP00000362779.4:p.Gly55Arg
ENST00000540630.6:c.163G>A	ENSP00000441668.3:p.Gly55Arg
ENST00000613327.5:c.163G>A	ENSP00000480757.2:p.Gly55Arg
ENST00000685006.1:c.235G>A	ENSP00000510318.1:p.Gly79Arg
ENST00000685060.1:n.400G>A
ENST00000685154.1:c.163G>A	ENSP00000509251.1:p.Gly55Arg
ENST00000685627.1:c.*174G>A	ENSP00000508637.1:n.*174G>A
ENST00000686289.1:n.113+15418G>A
ENST00000687572.1:c.-221+15418G>A	ENSP00000510427.1:n.-221+15418G>A
ENST00000687705.1:c.*412G>A	ENSP00000509639.1:n.*412G>A
ENST00000688812.1:c.163G>A	ENSP00000510658.1:p.Gly55Arg
ENST00000689218.1:n.392G>A
ENST00000689484.1:c.-220-21339G>A	ENSP00000509884.1:n.-220-21339G>A
ENST00000689797.1:c.-220-21339G>A	ENSP00000510689.1:n.-220-21339G>A
ENST00000690544.1:c.163G>A	ENSP00000508989.1:p.Gly55Arg
ENST00000692038.1:c.*412G>A	ENSP00000509220.1:n.*412G>A
ENST00000692953.1:n.62+15418G>A
ENST00000692979.1:c.163G>A	ENSP00000509849.1:p.Gly55Arg
ENST00000358913.10:c.163G>A MANE Select	ENSP00000351790.5:p.Gly55Arg
ENST00000354393.6:c.77+14800G>A	ENSP00000346369.2:n.77+14800G>A
ENST00000358913.9:c.163G>A	ENSP00000351790.5:p.Gly55Arg
ENST00000373675.3:c.163G>A	ENSP00000362779.3:p.Gly55Arg
ENST00000540630.5:c.163G>A	ENSP00000441668.2:p.Gly55Arg
ENST00000613327.4:c.-960G>A	ENSP00000480757.1:n.-960G>A
NM_001256267.1:c.163G>A	NP_001243196.1:p.Gly55Arg
NM_001256268.1:c.-960G>A	NP_001243197.1:n.-960G>A
NM_032578.3:c.163G>A , LRG_410t1:c.163G>A	NP_115967.2:p.Gly55Arg
NR_045662.3:n.329+14800G>A
NR_045663.3:n.455G>A
XM_006718043.2:c.163G>A	XP_006718106.1:p.Gly55Arg
XM_011540292.1:c.163G>A	XP_011538594.1:p.Gly55Arg
XM_017016833.1:c.241G>A	XP_016872322.1:p.Gly81Arg
XM_017016834.2:c.163G>A	XP_016872323.1:p.Gly55Arg
XM_024448236.1:c.-221+15418G>A	XP_024304004.1:n.-221+15418G>A
NR_045662.4:n.439+14800G>A
NR_045663.4:n.400G>A
NM_001256267.2:c.163G>A	NP_001243196.1:p.Gly55Arg
NM_001256268.2:c.-960G>A	NP_001243197.1:n.-960G>A
NM_032578.4:c.163G>A MANE Select	NP_115967.2:p.Gly55Arg