Canonical Allele Identifier: CA376838471

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69925557G>A (hg19) ; chr10:g.68165800G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165800G>A , CM000672.2:g.68165800G>A	GRCh38
NC_000010.10:g.69925557G>A , CM000672.1:g.69925557G>A	GRCh37
NC_000010.9:g.69595563G>A	NCBI36
NG_032118.1:g.64684G>A , LRG_410:g.64684G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.757G>A	ENSP00000346369.2:p.Ala253Thr
ENST00000373675.4:c.1582G>A	ENSP00000362779.4:p.Ala528Thr
ENST00000540630.6:c.1636G>A	ENSP00000441668.3:p.Ala546Thr
ENST00000613327.5:c.1582G>A	ENSP00000480757.2:p.Ala528Thr
ENST00000687572.1:c.460G>A	ENSP00000510427.1:p.Ala154Thr
ENST00000687705.1:c.*1831G>A	ENSP00000509639.1:n.*1831G>A
ENST00000688812.1:c.1558G>A	ENSP00000510658.1:p.Ala520Thr
ENST00000689002.1:n.634G>A
ENST00000690544.1:c.*853G>A	ENSP00000508989.1:n.*853G>A
ENST00000358913.10:c.1582G>A MANE Select	ENSP00000351790.5:p.Ala528Thr
ENST00000354393.6:c.757G>A	ENSP00000346369.2:p.Ala253Thr
ENST00000358913.9:c.1582G>A	ENSP00000351790.5:p.Ala528Thr
ENST00000540630.5:c.1582G>A	ENSP00000441668.2:p.Ala528Thr
ENST00000613327.4:c.700G>A	ENSP00000480757.1:p.Ala234Thr
NM_001256267.1:c.1582G>A	NP_001243196.1:p.Ala528Thr
NM_001256268.1:c.700G>A	NP_001243197.1:p.Ala234Thr
NM_032578.3:c.1582G>A , LRG_410t1:c.1582G>A	NP_115967.2:p.Ala528Thr
NR_045662.3:n.1009G>A
NR_045663.3:n.1850G>A
XM_006718043.2:c.1636G>A	XP_006718106.1:p.Ala546Thr
XM_011540292.1:c.1612G>A	XP_011538594.1:p.Ala538Thr
XM_017016833.1:c.1660G>A	XP_016872322.1:p.Ala554Thr
XM_017016834.2:c.1582G>A	XP_016872323.1:p.Ala528Thr
XM_024448236.1:c.460G>A	XP_024304004.1:p.Ala154Thr
NR_045662.4:n.1119G>A
NR_045663.4:n.1795G>A
NM_001256267.2:c.1582G>A	NP_001243196.1:p.Ala528Thr
NM_001256268.2:c.700G>A	NP_001243197.1:p.Ala234Thr
NM_032578.4:c.1582G>A MANE Select	NP_115967.2:p.Ala528Thr