Canonical Allele Identifier: CA469804580

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69925472C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165715C>T , CM000672.2:g.68165715C>T	GRCh38
NC_000010.10:g.69925472C>T , CM000672.1:g.69925472C>T	GRCh37
NC_000010.9:g.69595478C>T	NCBI36
NG_032118.1:g.64599C>T , LRG_410:g.64599C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.672C>T	ENSP00000346369.2:p.Thr224=
ENST00000373675.4:c.1497C>T	ENSP00000362779.4:p.Thr499=
ENST00000540630.6:c.1551C>T	ENSP00000441668.3:p.Thr517=
ENST00000613327.5:c.1497C>T	ENSP00000480757.2:p.Thr499=
ENST00000687572.1:c.375C>T	ENSP00000510427.1:p.Thr125=
ENST00000687705.1:c.*1746C>T	ENSP00000509639.1:n.*1746C>T
ENST00000688812.1:c.1473C>T	ENSP00000510658.1:p.Thr491=
ENST00000689002.1:n.549C>T
ENST00000690544.1:c.*768C>T	ENSP00000508989.1:n.*768C>T
ENST00000358913.10:c.1497C>T MANE Select	ENSP00000351790.5:p.Thr499=
ENST00000354393.6:c.672C>T	ENSP00000346369.2:p.Thr224=
ENST00000358913.9:c.1497C>T	ENSP00000351790.5:p.Thr499=
ENST00000540630.5:c.1497C>T	ENSP00000441668.2:p.Thr499=
ENST00000613327.4:c.615C>T	ENSP00000480757.1:p.Thr205=
NM_001256267.1:c.1497C>T	NP_001243196.1:p.Thr499=
NM_001256268.1:c.615C>T	NP_001243197.1:p.Thr205=
NM_032578.3:c.1497C>T , LRG_410t1:c.1497C>T	NP_115967.2:p.Thr499=
NR_045662.3:n.924C>T
NR_045663.3:n.1765C>T
XM_006718043.2:c.1551C>T	XP_006718106.1:p.Thr517=
XM_011540292.1:c.1527C>T	XP_011538594.1:p.Thr509=
XM_017016833.1:c.1575C>T	XP_016872322.1:p.Thr525=
XM_017016834.2:c.1497C>T	XP_016872323.1:p.Thr499=
XM_024448236.1:c.375C>T	XP_024304004.1:p.Thr125=
NR_045662.4:n.1034C>T
NR_045663.4:n.1710C>T
NM_001256267.2:c.1497C>T	NP_001243196.1:p.Thr499=
NM_001256268.2:c.615C>T	NP_001243197.1:p.Thr205=
NM_032578.4:c.1497C>T MANE Select	NP_115967.2:p.Thr499=