Canonical Allele Identifier: CA376839674

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926122C>A (hg19) ; chr10:g.68166365C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166365C>A , CM000672.2:g.68166365C>A	GRCh38
NC_000010.10:g.69926122C>A , CM000672.1:g.69926122C>A	GRCh37
NC_000010.9:g.69596128C>A	NCBI36
NG_032118.1:g.65249C>A , LRG_410:g.65249C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.847C>A	ENSP00000346369.2:p.Pro283Thr
ENST00000373675.4:c.1672C>A	ENSP00000362779.4:p.Pro558Thr
ENST00000540630.6:c.1726C>A	ENSP00000441668.3:p.Pro576Thr
ENST00000613327.5:c.1672C>A	ENSP00000480757.2:p.Pro558Thr
ENST00000687572.1:c.550C>A	ENSP00000510427.1:p.Pro184Thr
ENST00000687705.1:c.*1921C>A	ENSP00000509639.1:n.*1921C>A
ENST00000688812.1:c.1648C>A	ENSP00000510658.1:p.Pro550Thr
ENST00000689002.1:n.724C>A
ENST00000690544.1:c.*943C>A	ENSP00000508989.1:n.*943C>A
ENST00000358913.10:c.1672C>A MANE Select	ENSP00000351790.5:p.Pro558Thr
ENST00000354393.6:c.847C>A	ENSP00000346369.2:p.Pro283Thr
ENST00000358913.9:c.1672C>A	ENSP00000351790.5:p.Pro558Thr
ENST00000540630.5:c.1672C>A	ENSP00000441668.2:p.Pro558Thr
ENST00000613327.4:c.790C>A	ENSP00000480757.1:p.Pro264Thr
NM_001256267.1:c.1672C>A	NP_001243196.1:p.Pro558Thr
NM_001256268.1:c.790C>A	NP_001243197.1:p.Pro264Thr
NM_032578.3:c.1672C>A , LRG_410t1:c.1672C>A	NP_115967.2:p.Pro558Thr
NR_045662.3:n.1099C>A
NR_045663.3:n.1940C>A
XM_006718043.2:c.1726C>A	XP_006718106.1:p.Pro576Thr
XM_011540292.1:c.1702C>A	XP_011538594.1:p.Pro568Thr
XM_017016833.1:c.1750C>A	XP_016872322.1:p.Pro584Thr
XM_017016834.2:c.1672C>A	XP_016872323.1:p.Pro558Thr
XM_024448236.1:c.550C>A	XP_024304004.1:p.Pro184Thr
NR_045662.4:n.1209C>A
NR_045663.4:n.1885C>A
NM_001256267.2:c.1672C>A	NP_001243196.1:p.Pro558Thr
NM_001256268.2:c.790C>A	NP_001243197.1:p.Pro264Thr
NM_032578.4:c.1672C>A MANE Select	NP_115967.2:p.Pro558Thr