Canonical Allele Identifier: CA1917232527

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210597_68210598delinsCA , CM000672.2:g.68210597_68210598delinsCA	GRCh38
NC_000010.10:g.69970354_69970355delinsCA , CM000672.1:g.69970354_69970355delinsCA	GRCh37
NC_000010.9:g.69640360_69640361delinsCA	NCBI36
NG_032118.1:g.109481_109482delinsCA , LRG_410:g.109481_109482delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.*142_*143delinsCA	ENSP00000346369.2:n.*142_*143delinsCA
ENST00000540630.6:c.*142_*143delinsCA	ENSP00000441668.3:n.*142_*143delinsCA
ENST00000613327.5:c.*142_*143delinsCA	ENSP00000480757.2:n.*142_*143delinsCA
ENST00000688812.1:c.*1368_*1369delinsCA	ENSP00000510658.1:n.*1368_*1369delinsCA
ENST00000690544.1:c.*3376_*3377delinsCA	ENSP00000508989.1:n.*3376_*3377delinsCA
ENST00000358913.10:c.*142_*143delinsCA MANE Select	ENSP00000351790.5:n.*142_*143delinsCA
ENST00000354393.6:c.*142_*143delinsCA	ENSP00000346369.2:n.*142_*143delinsCA
ENST00000358913.9:c.*142_*143delinsCA	ENSP00000351790.5:n.*142_*143delinsCA
ENST00000540630.5:c.*142_*143delinsCA	ENSP00000441668.2:n.*142_*143delinsCA
ENST00000613327.4:c.*142_*143delinsCA	ENSP00000480757.1:n.*142_*143delinsCA
NM_001256267.1:c.*142_*143delinsCA	NP_001243196.1:n.*142_*143delinsCA
NM_001256268.1:c.*142_*143delinsCA	NP_001243197.1:n.*142_*143delinsCA
NM_032578.3:c.*142_*143delinsCA , LRG_410t1:c.*142_*143delinsCA	NP_115967.2:n.*142_*143delinsCA
NR_045662.3:n.3532_3533delinsCA
NR_045663.3:n.4234_4235delinsCA
XM_006718043.2:c.*142_*143delinsCA	XP_006718106.1:n.*142_*143delinsCA
XM_011540292.1:c.*142_*143delinsCA	XP_011538594.1:n.*142_*143delinsCA
XR_946029.1:n.1574+4690_1574+4691delinsTG
XM_017016833.1:c.*142_*143delinsCA	XP_016872322.1:n.*142_*143delinsCA
XM_017016834.2:c.*142_*143delinsCA	XP_016872323.1:n.*142_*143delinsCA
XM_024448236.1:c.*142_*143delinsCA	XP_024304004.1:n.*142_*143delinsCA
NR_045662.4:n.3642_3643delinsCA
NR_045663.4:n.4179_4180delinsCA
NM_001256267.2:c.*142_*143delinsCA	NP_001243196.1:n.*142_*143delinsCA
NM_001256268.2:c.*142_*143delinsCA	NP_001243197.1:n.*142_*143delinsCA
NM_032578.4:c.*142_*143delinsCA MANE Select	NP_115967.2:n.*142_*143delinsCA