Canonical Allele Identifier: CA376857659

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69955273G>A (hg19) ; chr10:g.68195516G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195516G>A , CM000672.2:g.68195516G>A	GRCh38
NC_000010.10:g.69955273G>A , CM000672.1:g.69955273G>A	GRCh37
NC_000010.9:g.69625279G>A	NCBI36
NG_032118.1:g.94400G>A , LRG_410:g.94400G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2317G>A	ENSP00000346369.2:p.Ala773Thr
ENST00000540630.6:c.3196G>A	ENSP00000441668.3:p.Ala1066Thr
ENST00000613327.5:c.3142G>A	ENSP00000480757.2:p.Ala1048Thr
ENST00000688812.1:c.*405G>A	ENSP00000510658.1:n.*405G>A
ENST00000690544.1:c.*2413G>A	ENSP00000508989.1:n.*2413G>A
ENST00000358913.10:c.3142G>A MANE Select	ENSP00000351790.5:p.Ala1048Thr
ENST00000354393.6:c.2317G>A	ENSP00000346369.2:p.Ala773Thr
ENST00000358913.9:c.3142G>A	ENSP00000351790.5:p.Ala1048Thr
ENST00000540630.5:c.3142G>A	ENSP00000441668.2:p.Ala1048Thr
ENST00000613327.4:c.2260G>A	ENSP00000480757.1:p.Ala754Thr
NM_001256267.1:c.3142G>A	NP_001243196.1:p.Ala1048Thr
NM_001256268.1:c.2260G>A	NP_001243197.1:p.Ala754Thr
NM_032578.3:c.3142G>A , LRG_410t1:c.3142G>A	NP_115967.2:p.Ala1048Thr
NR_045662.3:n.2569G>A
NR_045663.3:n.3271G>A
XM_006718043.2:c.3196G>A	XP_006718106.1:p.Ala1066Thr
XM_011540292.1:c.3172G>A	XP_011538594.1:p.Ala1058Thr
XM_017016833.1:c.3220G>A	XP_016872322.1:p.Ala1074Thr
XM_017016834.2:c.3142G>A	XP_016872323.1:p.Ala1048Thr
XM_024448236.1:c.2020G>A	XP_024304004.1:p.Ala674Thr
NR_045662.4:n.2679G>A
NR_045663.4:n.3216G>A
NM_001256267.2:c.3142G>A	NP_001243196.1:p.Ala1048Thr
NM_001256268.2:c.2260G>A	NP_001243197.1:p.Ala754Thr
NM_032578.4:c.3142G>A MANE Select	NP_115967.2:p.Ala1048Thr