Canonical Allele Identifier: CA1917225722

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195789_68195791delinsGCT , CM000672.2:g.68195789_68195791delinsGCT	GRCh38
NC_000010.10:g.69955546_69955548delinsGCT , CM000672.1:g.69955546_69955548delinsGCT	GRCh37
NC_000010.9:g.69625552_69625554delinsGCT	NCBI36
NG_032118.1:g.94673_94675delinsGCT , LRG_410:g.94673_94675delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2333+257_2333+259delinsGCT	ENSP00000346369.2:n.2333+257_2333+259delinsGCT
ENST00000540630.6:c.3212+257_3212+259delinsGCT	ENSP00000441668.3:n.3212+257_3212+259delinsGCT
ENST00000613327.5:c.3158+257_3158+259delinsGCT	ENSP00000480757.2:n.3158+257_3158+259delinsGCT
ENST00000688812.1:c.*421+257_*421+259delinsGCT	ENSP00000510658.1:n.*421+257_*421+259delinsGCT
ENST00000690544.1:c.*2429+257_*2429+259delinsGCT	ENSP00000508989.1:n.*2429+257_*2429+259delinsGCT
ENST00000358913.10:c.3158+257_3158+259delinsGCT MANE Select	ENSP00000351790.5:n.3158+257_3158+259delinsGCT
ENST00000354393.6:c.2333+257_2333+259delinsGCT	ENSP00000346369.2:n.2333+257_2333+259delinsGCT
ENST00000358913.9:c.3158+257_3158+259delinsGCT	ENSP00000351790.5:n.3158+257_3158+259delinsGCT
ENST00000540630.5:c.3158+257_3158+259delinsGCT	ENSP00000441668.2:n.3158+257_3158+259delinsGCT
ENST00000613327.4:c.2276+257_2276+259delinsGCT	ENSP00000480757.1:n.2276+257_2276+259delinsGCT
NM_001256267.1:c.3158+257_3158+259delinsGCT	NP_001243196.1:n.3158+257_3158+259delinsGCT
NM_001256268.1:c.2276+257_2276+259delinsGCT	NP_001243197.1:n.2276+257_2276+259delinsGCT
NM_032578.3:c.3158+257_3158+259delinsGCT , LRG_410t1:c.3158+257_3158+259delinsGCT	NP_115967.2:n.3158+257_3158+259delinsGCT
NR_045662.3:n.2585+257_2585+259delinsGCT
NR_045663.3:n.3287+257_3287+259delinsGCT
XM_006718043.2:c.3212+257_3212+259delinsGCT	XP_006718106.1:n.3212+257_3212+259delinsGCT
XM_011540292.1:c.3188+257_3188+259delinsGCT	XP_011538594.1:n.3188+257_3188+259delinsGCT
XM_017016833.1:c.3236+257_3236+259delinsGCT	XP_016872322.1:n.3236+257_3236+259delinsGCT
XM_017016834.2:c.3158+257_3158+259delinsGCT	XP_016872323.1:n.3158+257_3158+259delinsGCT
XM_024448236.1:c.2036+257_2036+259delinsGCT	XP_024304004.1:n.2036+257_2036+259delinsGCT
NR_045662.4:n.2695+257_2695+259delinsGCT
NR_045663.4:n.3232+257_3232+259delinsGCT
NM_001256267.2:c.3158+257_3158+259delinsGCT	NP_001243196.1:n.3158+257_3158+259delinsGCT
NM_001256268.2:c.2276+257_2276+259delinsGCT	NP_001243197.1:n.2276+257_2276+259delinsGCT
NM_032578.4:c.3158+257_3158+259delinsGCT MANE Select	NP_115967.2:n.3158+257_3158+259delinsGCT