Canonical Allele Identifier: CA376837680

Gene: MYPN

Linked Data

• COSMIC: COSM332554
• MyVariant Identifiers: chr10:g.69925471C>A (hg19) ; chr10:g.68165714C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165714C>A , CM000672.2:g.68165714C>A	GRCh38
NC_000010.10:g.69925471C>A , CM000672.1:g.69925471C>A	GRCh37
NC_000010.9:g.69595477C>A	NCBI36
NG_032118.1:g.64598C>A , LRG_410:g.64598C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000354393.7:c.671C>A	ENSP00000346369.2:p.Thr224Asn
ENST00000373675.4:c.1496C>A	ENSP00000362779.4:p.Thr499Asn
ENST00000540630.6:c.1550C>A	ENSP00000441668.3:p.Thr517Asn
ENST00000613327.5:c.1496C>A	ENSP00000480757.2:p.Thr499Asn
ENST00000687572.1:c.374C>A	ENSP00000510427.1:p.Thr125Asn
ENST00000687705.1:c.*1745C>A	ENSP00000509639.1:n.*1745C>A
ENST00000688812.1:c.1472C>A	ENSP00000510658.1:p.Thr491Asn
ENST00000689002.1:n.548C>A
ENST00000690544.1:c.*767C>A	ENSP00000508989.1:n.*767C>A
ENST00000358913.10:c.1496C>A MANE Select	ENSP00000351790.5:p.Thr499Asn
ENST00000354393.6:c.671C>A	ENSP00000346369.2:p.Thr224Asn
ENST00000358913.9:c.1496C>A	ENSP00000351790.5:p.Thr499Asn
ENST00000540630.5:c.1496C>A	ENSP00000441668.2:p.Thr499Asn
ENST00000613327.4:c.614C>A	ENSP00000480757.1:p.Thr205Asn
NM_001256267.1:c.1496C>A	NP_001243196.1:p.Thr499Asn
NM_001256268.1:c.614C>A	NP_001243197.1:p.Thr205Asn
NM_032578.3:c.1496C>A , LRG_410t1:c.1496C>A	NP_115967.2:p.Thr499Asn
NR_045662.3:n.923C>A
NR_045663.3:n.1764C>A
XM_006718043.2:c.1550C>A	XP_006718106.1:p.Thr517Asn
XM_011540292.1:c.1526C>A	XP_011538594.1:p.Thr509Asn
XM_017016833.1:c.1574C>A	XP_016872322.1:p.Thr525Asn
XM_017016834.2:c.1496C>A	XP_016872323.1:p.Thr499Asn
XM_024448236.1:c.374C>A	XP_024304004.1:p.Thr125Asn
NR_045662.4:n.1033C>A
NR_045663.4:n.1709C>A
NM_001256267.2:c.1496C>A	NP_001243196.1:p.Thr499Asn
NM_001256268.2:c.614C>A	NP_001243197.1:p.Thr205Asn
NM_032578.4:c.1496C>A MANE Select	NP_115967.2:p.Thr499Asn