Canonical Allele Identifier: CA2788367487

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195798_68195799del , CM000672.2:g.68195798_68195799del	GRCh38
NC_000010.10:g.69955555_69955556del , CM000672.1:g.69955555_69955556del	GRCh37
NC_000010.9:g.69625561_69625562del	NCBI36
NG_032118.1:g.94682_94683del , LRG_410:g.94682_94683del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2333+266_2333+267del	ENSP00000346369.2:n.2333+266_2333+267del
ENST00000540630.6:c.3212+266_3212+267del	ENSP00000441668.3:n.3212+266_3212+267del
ENST00000613327.5:c.3158+266_3158+267del	ENSP00000480757.2:n.3158+266_3158+267del
ENST00000688812.1:c.*421+266_*421+267del	ENSP00000510658.1:n.*421+266_*421+267del
ENST00000690544.1:c.*2429+266_*2429+267del	ENSP00000508989.1:n.*2429+266_*2429+267del
ENST00000358913.10:c.3158+266_3158+267del MANE Select	ENSP00000351790.5:n.3158+266_3158+267del
ENST00000354393.6:c.2333+266_2333+267del	ENSP00000346369.2:n.2333+266_2333+267del
ENST00000358913.9:c.3158+266_3158+267del	ENSP00000351790.5:n.3158+266_3158+267del
ENST00000540630.5:c.3158+266_3158+267del	ENSP00000441668.2:n.3158+266_3158+267del
ENST00000613327.4:c.2276+266_2276+267del	ENSP00000480757.1:n.2276+266_2276+267del
NM_001256267.1:c.3158+266_3158+267del	NP_001243196.1:n.3158+266_3158+267del
NM_001256268.1:c.2276+266_2276+267del	NP_001243197.1:n.2276+266_2276+267del
NM_032578.3:c.3158+266_3158+267del , LRG_410t1:c.3158+266_3158+267del	NP_115967.2:n.3158+266_3158+267del
NR_045662.3:n.2585+266_2585+267del
NR_045663.3:n.3287+266_3287+267del
XM_006718043.2:c.3212+266_3212+267del	XP_006718106.1:n.3212+266_3212+267del
XM_011540292.1:c.3188+266_3188+267del	XP_011538594.1:n.3188+266_3188+267del
XM_017016833.1:c.3236+266_3236+267del	XP_016872322.1:n.3236+266_3236+267del
XM_017016834.2:c.3158+266_3158+267del	XP_016872323.1:n.3158+266_3158+267del
XM_024448236.1:c.2036+266_2036+267del	XP_024304004.1:n.2036+266_2036+267del
NR_045662.4:n.2695+266_2695+267del
NR_045663.4:n.3232+266_3232+267del
NM_001256267.2:c.3158+266_3158+267del	NP_001243196.1:n.3158+266_3158+267del
NM_001256268.2:c.2276+266_2276+267del	NP_001243197.1:n.2276+266_2276+267del
NM_032578.4:c.3158+266_3158+267del MANE Select	NP_115967.2:n.3158+266_3158+267del