Canonical Allele Identifier: CA376838013

Gene: MYPN

Linked Data

• COSMIC: COSM1216503
• MyVariant Identifiers: chr10:g.69925507G>A (hg19) ; chr10:g.68165750G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165750G>A , CM000672.2:g.68165750G>A	GRCh38
NC_000010.10:g.69925507G>A , CM000672.1:g.69925507G>A	GRCh37
NC_000010.9:g.69595513G>A	NCBI36
NG_032118.1:g.64634G>A , LRG_410:g.64634G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.707G>A	ENSP00000346369.2:p.Gly236Glu
ENST00000373675.4:c.1532G>A	ENSP00000362779.4:p.Gly511Glu
ENST00000540630.6:c.1586G>A	ENSP00000441668.3:p.Gly529Glu
ENST00000613327.5:c.1532G>A	ENSP00000480757.2:p.Gly511Glu
ENST00000687572.1:c.410G>A	ENSP00000510427.1:p.Gly137Glu
ENST00000687705.1:c.*1781G>A	ENSP00000509639.1:n.*1781G>A
ENST00000688812.1:c.1508G>A	ENSP00000510658.1:p.Gly503Glu
ENST00000689002.1:n.584G>A
ENST00000690544.1:c.*803G>A	ENSP00000508989.1:n.*803G>A
ENST00000358913.10:c.1532G>A MANE Select	ENSP00000351790.5:p.Gly511Glu
ENST00000354393.6:c.707G>A	ENSP00000346369.2:p.Gly236Glu
ENST00000358913.9:c.1532G>A	ENSP00000351790.5:p.Gly511Glu
ENST00000540630.5:c.1532G>A	ENSP00000441668.2:p.Gly511Glu
ENST00000613327.4:c.650G>A	ENSP00000480757.1:p.Gly217Glu
NM_001256267.1:c.1532G>A	NP_001243196.1:p.Gly511Glu
NM_001256268.1:c.650G>A	NP_001243197.1:p.Gly217Glu
NM_032578.3:c.1532G>A , LRG_410t1:c.1532G>A	NP_115967.2:p.Gly511Glu
NR_045662.3:n.959G>A
NR_045663.3:n.1800G>A
XM_006718043.2:c.1586G>A	XP_006718106.1:p.Gly529Glu
XM_011540292.1:c.1562G>A	XP_011538594.1:p.Gly521Glu
XM_017016833.1:c.1610G>A	XP_016872322.1:p.Gly537Glu
XM_017016834.2:c.1532G>A	XP_016872323.1:p.Gly511Glu
XM_024448236.1:c.410G>A	XP_024304004.1:p.Gly137Glu
NR_045662.4:n.1069G>A
NR_045663.4:n.1745G>A
NM_001256267.2:c.1532G>A	NP_001243196.1:p.Gly511Glu
NM_001256268.2:c.650G>A	NP_001243197.1:p.Gly217Glu
NM_032578.4:c.1532G>A MANE Select	NP_115967.2:p.Gly511Glu