Canonical Allele Identifier: CA469805708

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926139C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166382C>T , CM000672.2:g.68166382C>T	GRCh38
NC_000010.10:g.69926139C>T , CM000672.1:g.69926139C>T	GRCh37
NC_000010.9:g.69596145C>T	NCBI36
NG_032118.1:g.65266C>T , LRG_410:g.65266C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.864C>T	ENSP00000346369.2:p.Pro288=
ENST00000373675.4:c.1689C>T	ENSP00000362779.4:p.Pro563=
ENST00000540630.6:c.1743C>T	ENSP00000441668.3:p.Pro581=
ENST00000613327.5:c.1689C>T	ENSP00000480757.2:p.Pro563=
ENST00000687572.1:c.567C>T	ENSP00000510427.1:p.Pro189=
ENST00000688812.1:c.1665C>T	ENSP00000510658.1:p.Pro555=
ENST00000689002.1:n.741C>T
ENST00000690544.1:c.*960C>T	ENSP00000508989.1:n.*960C>T
ENST00000358913.10:c.1689C>T MANE Select	ENSP00000351790.5:p.Pro563=
ENST00000354393.6:c.864C>T	ENSP00000346369.2:p.Pro288=
ENST00000358913.9:c.1689C>T	ENSP00000351790.5:p.Pro563=
ENST00000540630.5:c.1689C>T	ENSP00000441668.2:p.Pro563=
ENST00000613327.4:c.807C>T	ENSP00000480757.1:p.Pro269=
NM_001256267.1:c.1689C>T	NP_001243196.1:p.Pro563=
NM_001256268.1:c.807C>T	NP_001243197.1:p.Pro269=
NM_032578.3:c.1689C>T , LRG_410t1:c.1689C>T	NP_115967.2:p.Pro563=
NR_045662.3:n.1116C>T
NR_045663.3:n.1957C>T
XM_006718043.2:c.1743C>T	XP_006718106.1:p.Pro581=
XM_011540292.1:c.1719C>T	XP_011538594.1:p.Pro573=
XM_017016833.1:c.1767C>T	XP_016872322.1:p.Pro589=
XM_017016834.2:c.1689C>T	XP_016872323.1:p.Pro563=
XM_024448236.1:c.567C>T	XP_024304004.1:p.Pro189=
NR_045662.4:n.1226C>T
NR_045663.4:n.1902C>T
NM_001256267.2:c.1689C>T	NP_001243196.1:p.Pro563=
NM_001256268.2:c.807C>T	NP_001243197.1:p.Pro269=
NM_032578.4:c.1689C>T MANE Select	NP_115967.2:p.Pro563=