Canonical Allele Identifier: CA376839828

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926155T>A (hg19) ; chr10:g.68166398T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166398T>A , CM000672.2:g.68166398T>A	GRCh38
NC_000010.10:g.69926155T>A , CM000672.1:g.69926155T>A	GRCh37
NC_000010.9:g.69596161T>A	NCBI36
NG_032118.1:g.65282T>A , LRG_410:g.65282T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.880T>A	ENSP00000346369.2:p.Ser294Thr
ENST00000373675.4:c.1705T>A	ENSP00000362779.4:p.Ser569Thr
ENST00000540630.6:c.1759T>A	ENSP00000441668.3:p.Ser587Thr
ENST00000613327.5:c.1705T>A	ENSP00000480757.2:p.Ser569Thr
ENST00000687572.1:c.583T>A	ENSP00000510427.1:p.Ser195Thr
ENST00000688812.1:c.1681T>A	ENSP00000510658.1:p.Ser561Thr
ENST00000689002.1:n.757T>A
ENST00000690544.1:c.*976T>A	ENSP00000508989.1:n.*976T>A
ENST00000358913.10:c.1705T>A MANE Select	ENSP00000351790.5:p.Ser569Thr
ENST00000354393.6:c.880T>A	ENSP00000346369.2:p.Ser294Thr
ENST00000358913.9:c.1705T>A	ENSP00000351790.5:p.Ser569Thr
ENST00000540630.5:c.1705T>A	ENSP00000441668.2:p.Ser569Thr
ENST00000613327.4:c.823T>A	ENSP00000480757.1:p.Ser275Thr
NM_001256267.1:c.1705T>A	NP_001243196.1:p.Ser569Thr
NM_001256268.1:c.823T>A	NP_001243197.1:p.Ser275Thr
NM_032578.3:c.1705T>A , LRG_410t1:c.1705T>A	NP_115967.2:p.Ser569Thr
NR_045662.3:n.1132T>A
NR_045663.3:n.1973T>A
XM_006718043.2:c.1759T>A	XP_006718106.1:p.Ser587Thr
XM_011540292.1:c.1735T>A	XP_011538594.1:p.Ser579Thr
XM_017016833.1:c.1783T>A	XP_016872322.1:p.Ser595Thr
XM_017016834.2:c.1705T>A	XP_016872323.1:p.Ser569Thr
XM_024448236.1:c.583T>A	XP_024304004.1:p.Ser195Thr
NR_045662.4:n.1242T>A
NR_045663.4:n.1918T>A
NM_001256267.2:c.1705T>A	NP_001243196.1:p.Ser569Thr
NM_001256268.2:c.823T>A	NP_001243197.1:p.Ser275Thr
NM_032578.4:c.1705T>A MANE Select	NP_115967.2:p.Ser569Thr