Canonical Allele Identifier: CA376830451

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69970178C>T (hg19) ; chr10:g.68210421C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210421C>T , CM000672.2:g.68210421C>T	GRCh38
NC_000010.10:g.69970178C>T , CM000672.1:g.69970178C>T	GRCh37
NC_000010.9:g.69640184C>T	NCBI36
NG_032118.1:g.109305C>T , LRG_410:g.109305C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.3104C>T	ENSP00000346369.2:p.Ser1035Phe
ENST00000540630.6:c.3983C>T	ENSP00000441668.3:p.Ser1328Phe
ENST00000613327.5:c.3929C>T	ENSP00000480757.2:p.Ser1310Phe
ENST00000688812.1:c.*1192C>T	ENSP00000510658.1:n.*1192C>T
ENST00000690544.1:c.*3200C>T	ENSP00000508989.1:n.*3200C>T
ENST00000358913.10:c.3929C>T MANE Select	ENSP00000351790.5:p.Ser1310Phe
ENST00000354393.6:c.3104C>T	ENSP00000346369.2:p.Ser1035Phe
ENST00000358913.9:c.3929C>T	ENSP00000351790.5:p.Ser1310Phe
ENST00000540630.5:c.3929C>T	ENSP00000441668.2:p.Ser1310Phe
ENST00000613327.4:c.3047C>T	ENSP00000480757.1:p.Ser1016Phe
NM_001256267.1:c.3929C>T	NP_001243196.1:p.Ser1310Phe
NM_001256268.1:c.3047C>T	NP_001243197.1:p.Ser1016Phe
NM_032578.3:c.3929C>T , LRG_410t1:c.3929C>T	NP_115967.2:p.Ser1310Phe
NR_045662.3:n.3356C>T
NR_045663.3:n.4058C>T
XM_006718043.2:c.3983C>T	XP_006718106.1:p.Ser1328Phe
XM_011540292.1:c.3959C>T	XP_011538594.1:p.Ser1320Phe
XR_946029.1:n.1574+4867G>A
XM_017016833.1:c.4007C>T	XP_016872322.1:p.Ser1336Phe
XM_017016834.2:c.3929C>T	XP_016872323.1:p.Ser1310Phe
XM_024448236.1:c.2807C>T	XP_024304004.1:p.Ser936Phe
NR_045662.4:n.3466C>T
NR_045663.4:n.4003C>T
NM_001256267.2:c.3929C>T	NP_001243196.1:p.Ser1310Phe
NM_001256268.2:c.3047C>T	NP_001243197.1:p.Ser1016Phe
NM_032578.4:c.3929C>T MANE Select	NP_115967.2:p.Ser1310Phe