Canonical Allele Identifier: CA5522897

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68189144C>T , CM000672.2:g.68189144C>T	GRCh38
NC_000010.10:g.69948901C>T , CM000672.1:g.69948901C>T	GRCh37
NC_000010.9:g.69618907C>T	NCBI36
NG_032118.1:g.88028C>T , LRG_410:g.88028C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2100+18C>T	ENSP00000346369.2:n.2100+18C>T
ENST00000540630.6:c.2979+18C>T	ENSP00000441668.3:n.2979+18C>T
ENST00000613327.5:c.2925+18C>T	ENSP00000480757.2:n.2925+18C>T
ENST00000688812.1:c.*188+18C>T	ENSP00000510658.1:n.*188+18C>T
ENST00000690544.1:c.*2196+18C>T	ENSP00000508989.1:n.*2196+18C>T
ENST00000358913.10:c.2925+18C>T MANE Select	ENSP00000351790.5:n.2925+18C>T
ENST00000354393.6:c.2100+18C>T	ENSP00000346369.2:n.2100+18C>T
ENST00000358913.9:c.2925+18C>T	ENSP00000351790.5:n.2925+18C>T
ENST00000540630.5:c.2925+18C>T	ENSP00000441668.2:n.2925+18C>T
ENST00000613327.4:c.2043+18C>T	ENSP00000480757.1:n.2043+18C>T
NM_001256267.1:c.2925+18C>T	NP_001243196.1:n.2925+18C>T
NM_001256268.1:c.2043+18C>T	NP_001243197.1:n.2043+18C>T
NM_032578.3:c.2925+18C>T , LRG_410t1:c.2925+18C>T	NP_115967.2:n.2925+18C>T
NR_045662.3:n.2352+18C>T
NR_045663.3:n.3054+18C>T
XM_006718043.2:c.2979+18C>T	XP_006718106.1:n.2979+18C>T
XM_011540292.1:c.2955+18C>T	XP_011538594.1:n.2955+18C>T
XM_017016833.1:c.3003+18C>T	XP_016872322.1:n.3003+18C>T
XM_017016834.2:c.2925+18C>T	XP_016872323.1:n.2925+18C>T
XM_024448236.1:c.1803+18C>T	XP_024304004.1:n.1803+18C>T
NR_045662.4:n.2462+18C>T
NR_045663.4:n.2999+18C>T
NM_001256267.2:c.2925+18C>T	NP_001243196.1:n.2925+18C>T
NM_001256268.2:c.2043+18C>T	NP_001243197.1:n.2043+18C>T
NM_032578.4:c.2925+18C>T MANE Select	NP_115967.2:n.2925+18C>T