Canonical Allele Identifier: CA1917225716

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195785_68195786delinsTG , CM000672.2:g.68195785_68195786delinsTG	GRCh38
NC_000010.10:g.69955542_69955543delinsTG , CM000672.1:g.69955542_69955543delinsTG	GRCh37
NC_000010.9:g.69625548_69625549delinsTG	NCBI36
NG_032118.1:g.94669_94670delinsTG , LRG_410:g.94669_94670delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2333+253_2333+254delinsTG	ENSP00000346369.2:n.2333+253_2333+254delinsTG
ENST00000540630.6:c.3212+253_3212+254delinsTG	ENSP00000441668.3:n.3212+253_3212+254delinsTG
ENST00000613327.5:c.3158+253_3158+254delinsTG	ENSP00000480757.2:n.3158+253_3158+254delinsTG
ENST00000688812.1:c.*421+253_*421+254delinsTG	ENSP00000510658.1:n.*421+253_*421+254delinsTG
ENST00000690544.1:c.*2429+253_*2429+254delinsTG	ENSP00000508989.1:n.*2429+253_*2429+254delinsTG
ENST00000358913.10:c.3158+253_3158+254delinsTG MANE Select	ENSP00000351790.5:n.3158+253_3158+254delinsTG
ENST00000354393.6:c.2333+253_2333+254delinsTG	ENSP00000346369.2:n.2333+253_2333+254delinsTG
ENST00000358913.9:c.3158+253_3158+254delinsTG	ENSP00000351790.5:n.3158+253_3158+254delinsTG
ENST00000540630.5:c.3158+253_3158+254delinsTG	ENSP00000441668.2:n.3158+253_3158+254delinsTG
ENST00000613327.4:c.2276+253_2276+254delinsTG	ENSP00000480757.1:n.2276+253_2276+254delinsTG
NM_001256267.1:c.3158+253_3158+254delinsTG	NP_001243196.1:n.3158+253_3158+254delinsTG
NM_001256268.1:c.2276+253_2276+254delinsTG	NP_001243197.1:n.2276+253_2276+254delinsTG
NM_032578.3:c.3158+253_3158+254delinsTG , LRG_410t1:c.3158+253_3158+254delinsTG	NP_115967.2:n.3158+253_3158+254delinsTG
NR_045662.3:n.2585+253_2585+254delinsTG
NR_045663.3:n.3287+253_3287+254delinsTG
XM_006718043.2:c.3212+253_3212+254delinsTG	XP_006718106.1:n.3212+253_3212+254delinsTG
XM_011540292.1:c.3188+253_3188+254delinsTG	XP_011538594.1:n.3188+253_3188+254delinsTG
XM_017016833.1:c.3236+253_3236+254delinsTG	XP_016872322.1:n.3236+253_3236+254delinsTG
XM_017016834.2:c.3158+253_3158+254delinsTG	XP_016872323.1:n.3158+253_3158+254delinsTG
XM_024448236.1:c.2036+253_2036+254delinsTG	XP_024304004.1:n.2036+253_2036+254delinsTG
NR_045662.4:n.2695+253_2695+254delinsTG
NR_045663.4:n.3232+253_3232+254delinsTG
NM_001256267.2:c.3158+253_3158+254delinsTG	NP_001243196.1:n.3158+253_3158+254delinsTG
NM_001256268.2:c.2276+253_2276+254delinsTG	NP_001243197.1:n.2276+253_2276+254delinsTG
NM_032578.4:c.3158+253_3158+254delinsTG MANE Select	NP_115967.2:n.3158+253_3158+254delinsTG