Canonical Allele Identifier: CA469805188

Gene: MYPN

Linked Data

• COSMIC: COSM1297372
• MyVariant Identifiers: chr10:g.69925571G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165814G>C , CM000672.2:g.68165814G>C	GRCh38
NC_000010.10:g.69925571G>C , CM000672.1:g.69925571G>C	GRCh37
NC_000010.9:g.69595577G>C	NCBI36
NG_032118.1:g.64698G>C , LRG_410:g.64698G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.771G>C	ENSP00000346369.2:p.Val257=
ENST00000373675.4:c.1596G>C	ENSP00000362779.4:p.Val532=
ENST00000540630.6:c.1650G>C	ENSP00000441668.3:p.Val550=
ENST00000613327.5:c.1596G>C	ENSP00000480757.2:p.Val532=
ENST00000687572.1:c.474G>C	ENSP00000510427.1:p.Val158=
ENST00000687705.1:c.*1845G>C	ENSP00000509639.1:n.*1845G>C
ENST00000688812.1:c.1572G>C	ENSP00000510658.1:p.Val524=
ENST00000689002.1:n.648G>C
ENST00000690544.1:c.*867G>C	ENSP00000508989.1:n.*867G>C
ENST00000358913.10:c.1596G>C MANE Select	ENSP00000351790.5:p.Val532=
ENST00000354393.6:c.771G>C	ENSP00000346369.2:p.Val257=
ENST00000358913.9:c.1596G>C	ENSP00000351790.5:p.Val532=
ENST00000540630.5:c.1596G>C	ENSP00000441668.2:p.Val532=
ENST00000613327.4:c.714G>C	ENSP00000480757.1:p.Val238=
NM_001256267.1:c.1596G>C	NP_001243196.1:p.Val532=
NM_001256268.1:c.714G>C	NP_001243197.1:p.Val238=
NM_032578.3:c.1596G>C , LRG_410t1:c.1596G>C	NP_115967.2:p.Val532=
NR_045662.3:n.1023G>C
NR_045663.3:n.1864G>C
XM_006718043.2:c.1650G>C	XP_006718106.1:p.Val550=
XM_011540292.1:c.1626G>C	XP_011538594.1:p.Val542=
XM_017016833.1:c.1674G>C	XP_016872322.1:p.Val558=
XM_017016834.2:c.1596G>C	XP_016872323.1:p.Val532=
XM_024448236.1:c.474G>C	XP_024304004.1:p.Val158=
NR_045662.4:n.1133G>C
NR_045663.4:n.1809G>C
NM_001256267.2:c.1596G>C	NP_001243196.1:p.Val532=
NM_001256268.2:c.714G>C	NP_001243197.1:p.Val238=
NM_032578.4:c.1596G>C MANE Select	NP_115967.2:p.Val532=