Canonical Allele Identifier: CA2788377827

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166611_68166612insAACCACCAAACACACCCAACA , CM000672.2:g.68166611_68166612insAACCACCAAACACACCCAACA	GRCh38
NC_000010.10:g.69926368_69926369insAACCACCAAACACACCCAACA , CM000672.1:g.69926368_69926369insAACCACCAAACACACCCAACA	GRCh37
NC_000010.9:g.69596374_69596375insAACCACCAAACACACCCAACA	NCBI36
NG_032118.1:g.65495_65496insAACCACCAAACACACCCAACA , LRG_410:g.65495_65496insAACCACCAAACACACCCAACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1093_1094insAACCACCAAACACACCCAACA	ENSP00000346369.2:p.Pro365delinsGlnProProAsnThrProAsnThr
ENST00000373675.4:c.1918_1919insAACCACCAAACACACCCAACA	ENSP00000362779.4:p.Pro640delinsGlnProProAsnThrProAsnThr
ENST00000540630.6:c.1972_1973insAACCACCAAACACACCCAACA	ENSP00000441668.3:p.Pro658delinsGlnProProAsnThrProAsnThr
ENST00000613327.5:c.1918_1919insAACCACCAAACACACCCAACA	ENSP00000480757.2:p.Pro640delinsGlnProProAsnThrProAsnThr
ENST00000687572.1:c.796_797insAACCACCAAACACACCCAACA	ENSP00000510427.1:p.Pro266delinsGlnProProAsnThrProAsnThr
ENST00000688812.1:c.1894_1895insAACCACCAAACACACCCAACA	ENSP00000510658.1:p.Pro632delinsGlnProProAsnThrProAsnThr
ENST00000690544.1:c.*1189_*1190insAACCACCAAACACACCCAACA	ENSP00000508989.1:n.*1189_*1190insAACCACCAAACACACCCAACA
ENST00000358913.10:c.1918_1919insAACCACCAAACACACCCAACA MANE Select	ENSP00000351790.5:p.Pro640delinsGlnProProAsnThrProAsnThr
ENST00000354393.6:c.1093_1094insAACCACCAAACACACCCAACA	ENSP00000346369.2:p.Pro365delinsGlnProProAsnThrProAsnThr
ENST00000358913.9:c.1918_1919insAACCACCAAACACACCCAACA	ENSP00000351790.5:p.Pro640delinsGlnProProAsnThrProAsnThr
ENST00000540630.5:c.1918_1919insAACCACCAAACACACCCAACA	ENSP00000441668.2:p.Pro640delinsGlnProProAsnThrProAsnThr
ENST00000613327.4:c.1036_1037insAACCACCAAACACACCCAACA	ENSP00000480757.1:p.Pro346delinsGlnProProAsnThrProAsnThr
NM_001256267.1:c.1918_1919insAACCACCAAACACACCCAACA	NP_001243196.1:p.Pro640delinsGlnProProAsnThrProAsnThr
NM_001256268.1:c.1036_1037insAACCACCAAACACACCCAACA	NP_001243197.1:p.Pro346delinsGlnProProAsnThrProAsnThr
NM_032578.3:c.1918_1919insAACCACCAAACACACCCAACA , LRG_410t1:c.1918_1919insAACCACCAAACACACCCAACA	NP_115967.2:p.Pro640delinsGlnProProAsnThrProAsnThr
NR_045662.3:n.1345_1346insAACCACCAAACACACCCAACA
NR_045663.3:n.2186_2187insAACCACCAAACACACCCAACA
XM_006718043.2:c.1972_1973insAACCACCAAACACACCCAACA	XP_006718106.1:p.Pro658delinsGlnProProAsnThrProAsnThr
XM_011540292.1:c.1948_1949insAACCACCAAACACACCCAACA	XP_011538594.1:p.Pro650delinsGlnProProAsnThrProAsnThr
XM_017016833.1:c.1996_1997insAACCACCAAACACACCCAACA	XP_016872322.1:p.Pro666delinsGlnProProAsnThrProAsnThr
XM_017016834.2:c.1918_1919insAACCACCAAACACACCCAACA	XP_016872323.1:p.Pro640delinsGlnProProAsnThrProAsnThr
XM_024448236.1:c.796_797insAACCACCAAACACACCCAACA	XP_024304004.1:p.Pro266delinsGlnProProAsnThrProAsnThr
NR_045662.4:n.1455_1456insAACCACCAAACACACCCAACA
NR_045663.4:n.2131_2132insAACCACCAAACACACCCAACA
NM_001256267.2:c.1918_1919insAACCACCAAACACACCCAACA	NP_001243196.1:p.Pro640delinsGlnProProAsnThrProAsnThr
NM_001256268.2:c.1036_1037insAACCACCAAACACACCCAACA	NP_001243197.1:p.Pro346delinsGlnProProAsnThrProAsnThr
NM_032578.4:c.1918_1919insAACCACCAAACACACCCAACA MANE Select	NP_115967.2:p.Pro640delinsGlnProProAsnThrProAsnThr