Canonical Allele Identifier: CA376840457

Gene: MYPN

Linked Data

• COSMIC: COSM3439795 ; COSM3439796 ; COSM3439797
• MyVariant Identifiers: chr10:g.69926302G>A (hg19) ; chr10:g.68166545G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166545G>A , CM000672.2:g.68166545G>A	GRCh38
NC_000010.10:g.69926302G>A , CM000672.1:g.69926302G>A	GRCh37
NC_000010.9:g.69596308G>A	NCBI36
NG_032118.1:g.65429G>A , LRG_410:g.65429G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1027G>A	ENSP00000346369.2:p.Val343Met
ENST00000373675.4:c.1852G>A	ENSP00000362779.4:p.Val618Met
ENST00000540630.6:c.1906G>A	ENSP00000441668.3:p.Val636Met
ENST00000613327.5:c.1852G>A	ENSP00000480757.2:p.Val618Met
ENST00000687572.1:c.730G>A	ENSP00000510427.1:p.Val244Met
ENST00000688812.1:c.1828G>A	ENSP00000510658.1:p.Val610Met
ENST00000690544.1:c.*1123G>A	ENSP00000508989.1:n.*1123G>A
ENST00000358913.10:c.1852G>A MANE Select	ENSP00000351790.5:p.Val618Met
ENST00000354393.6:c.1027G>A	ENSP00000346369.2:p.Val343Met
ENST00000358913.9:c.1852G>A	ENSP00000351790.5:p.Val618Met
ENST00000540630.5:c.1852G>A	ENSP00000441668.2:p.Val618Met
ENST00000613327.4:c.970G>A	ENSP00000480757.1:p.Val324Met
NM_001256267.1:c.1852G>A	NP_001243196.1:p.Val618Met
NM_001256268.1:c.970G>A	NP_001243197.1:p.Val324Met
NM_032578.3:c.1852G>A , LRG_410t1:c.1852G>A	NP_115967.2:p.Val618Met
NR_045662.3:n.1279G>A
NR_045663.3:n.2120G>A
XM_006718043.2:c.1906G>A	XP_006718106.1:p.Val636Met
XM_011540292.1:c.1882G>A	XP_011538594.1:p.Val628Met
XM_017016833.1:c.1930G>A	XP_016872322.1:p.Val644Met
XM_017016834.2:c.1852G>A	XP_016872323.1:p.Val618Met
XM_024448236.1:c.730G>A	XP_024304004.1:p.Val244Met
NR_045662.4:n.1389G>A
NR_045663.4:n.2065G>A
NM_001256267.2:c.1852G>A	NP_001243196.1:p.Val618Met
NM_001256268.2:c.970G>A	NP_001243197.1:p.Val324Met
NM_032578.4:c.1852G>A MANE Select	NP_115967.2:p.Val618Met