Canonical Allele Identifier: CA1917225596

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195540_68195544delinsCAGTA , CM000672.2:g.68195540_68195544delinsCAGTA	GRCh38
NC_000010.10:g.69955297_69955301delinsCAGTA , CM000672.1:g.69955297_69955301delinsCAGTA	GRCh37
NC_000010.9:g.69625303_69625307delinsCAGTA	NCBI36
NG_032118.1:g.94424_94428delinsCAGTA , LRG_410:g.94424_94428delinsCAGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2333+8_2333+12delinsCAGTA	ENSP00000346369.2:n.2333+8_2333+12delinsCAGTA
ENST00000540630.6:c.3212+8_3212+12delinsCAGTA	ENSP00000441668.3:n.3212+8_3212+12delinsCAGTA
ENST00000613327.5:c.3158+8_3158+12delinsCAGTA	ENSP00000480757.2:n.3158+8_3158+12delinsCAGTA
ENST00000688812.1:c.*421+8_*421+12delinsCAGTA	ENSP00000510658.1:n.*421+8_*421+12delinsCAGTA
ENST00000690544.1:c.*2429+8_*2429+12delinsCAGTA	ENSP00000508989.1:n.*2429+8_*2429+12delinsCAGTA
ENST00000358913.10:c.3158+8_3158+12delinsCAGTA MANE Select	ENSP00000351790.5:n.3158+8_3158+12delinsCAGTA
ENST00000354393.6:c.2333+8_2333+12delinsCAGTA	ENSP00000346369.2:n.2333+8_2333+12delinsCAGTA
ENST00000358913.9:c.3158+8_3158+12delinsCAGTA	ENSP00000351790.5:n.3158+8_3158+12delinsCAGTA
ENST00000540630.5:c.3158+8_3158+12delinsCAGTA	ENSP00000441668.2:n.3158+8_3158+12delinsCAGTA
ENST00000613327.4:c.2276+8_2276+12delinsCAGTA	ENSP00000480757.1:n.2276+8_2276+12delinsCAGTA
NM_001256267.1:c.3158+8_3158+12delinsCAGTA	NP_001243196.1:n.3158+8_3158+12delinsCAGTA
NM_001256268.1:c.2276+8_2276+12delinsCAGTA	NP_001243197.1:n.2276+8_2276+12delinsCAGTA
NM_032578.3:c.3158+8_3158+12delinsCAGTA , LRG_410t1:c.3158+8_3158+12delinsCAGTA	NP_115967.2:n.3158+8_3158+12delinsCAGTA
NR_045662.3:n.2585+8_2585+12delinsCAGTA
NR_045663.3:n.3287+8_3287+12delinsCAGTA
XM_006718043.2:c.3212+8_3212+12delinsCAGTA	XP_006718106.1:n.3212+8_3212+12delinsCAGTA
XM_011540292.1:c.3188+8_3188+12delinsCAGTA	XP_011538594.1:n.3188+8_3188+12delinsCAGTA
XM_017016833.1:c.3236+8_3236+12delinsCAGTA	XP_016872322.1:n.3236+8_3236+12delinsCAGTA
XM_017016834.2:c.3158+8_3158+12delinsCAGTA	XP_016872323.1:n.3158+8_3158+12delinsCAGTA
XM_024448236.1:c.2036+8_2036+12delinsCAGTA	XP_024304004.1:n.2036+8_2036+12delinsCAGTA
NR_045662.4:n.2695+8_2695+12delinsCAGTA
NR_045663.4:n.3232+8_3232+12delinsCAGTA
NM_001256267.2:c.3158+8_3158+12delinsCAGTA	NP_001243196.1:n.3158+8_3158+12delinsCAGTA
NM_001256268.2:c.2276+8_2276+12delinsCAGTA	NP_001243197.1:n.2276+8_2276+12delinsCAGTA
NM_032578.4:c.3158+8_3158+12delinsCAGTA MANE Select	NP_115967.2:n.3158+8_3158+12delinsCAGTA