Canonical Allele Identifier: CA2560015451

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195870A>T , CM000672.2:g.68195870A>T	GRCh38
NC_000010.10:g.69955627A>T , CM000672.1:g.69955627A>T	GRCh37
NC_000010.9:g.69625633A>T	NCBI36
NG_032118.1:g.94754A>T , LRG_410:g.94754A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2333+338A>T	ENSP00000346369.2:n.2333+338A>T
ENST00000540630.6:c.3212+338A>T	ENSP00000441668.3:n.3212+338A>T
ENST00000613327.5:c.3158+338A>T	ENSP00000480757.2:n.3158+338A>T
ENST00000688812.1:c.*421+338A>T	ENSP00000510658.1:n.*421+338A>T
ENST00000690544.1:c.*2429+338A>T	ENSP00000508989.1:n.*2429+338A>T
ENST00000358913.10:c.3158+338A>T MANE Select	ENSP00000351790.5:n.3158+338A>T
ENST00000354393.6:c.2333+338A>T	ENSP00000346369.2:n.2333+338A>T
ENST00000358913.9:c.3158+338A>T	ENSP00000351790.5:n.3158+338A>T
ENST00000540630.5:c.3158+338A>T	ENSP00000441668.2:n.3158+338A>T
ENST00000613327.4:c.2276+338A>T	ENSP00000480757.1:n.2276+338A>T
NM_001256267.1:c.3158+338A>T	NP_001243196.1:n.3158+338A>T
NM_001256268.1:c.2276+338A>T	NP_001243197.1:n.2276+338A>T
NM_032578.3:c.3158+338A>T , LRG_410t1:c.3158+338A>T	NP_115967.2:n.3158+338A>T
NR_045662.3:n.2585+338A>T
NR_045663.3:n.3287+338A>T
XM_006718043.2:c.3212+338A>T	XP_006718106.1:n.3212+338A>T
XM_011540292.1:c.3188+338A>T	XP_011538594.1:n.3188+338A>T
XM_017016833.1:c.3236+338A>T	XP_016872322.1:n.3236+338A>T
XM_017016834.2:c.3158+338A>T	XP_016872323.1:n.3158+338A>T
XM_024448236.1:c.2036+338A>T	XP_024304004.1:n.2036+338A>T
NR_045662.4:n.2695+338A>T
NR_045663.4:n.3232+338A>T
NM_001256267.2:c.3158+338A>T	NP_001243196.1:n.3158+338A>T
NM_001256268.2:c.2276+338A>T	NP_001243197.1:n.2276+338A>T
NM_032578.4:c.3158+338A>T MANE Select	NP_115967.2:n.3158+338A>T