Canonical Allele Identifier: CA376840756

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926357C>T (hg19) ; chr10:g.68166600C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166600C>T , CM000672.2:g.68166600C>T	GRCh38
NC_000010.10:g.69926357C>T , CM000672.1:g.69926357C>T	GRCh37
NC_000010.9:g.69596363C>T	NCBI36
NG_032118.1:g.65484C>T , LRG_410:g.65484C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1082C>T	ENSP00000346369.2:p.Ala361Val
ENST00000373675.4:c.1907C>T	ENSP00000362779.4:p.Ala636Val
ENST00000540630.6:c.1961C>T	ENSP00000441668.3:p.Ala654Val
ENST00000613327.5:c.1907C>T	ENSP00000480757.2:p.Ala636Val
ENST00000687572.1:c.785C>T	ENSP00000510427.1:p.Ala262Val
ENST00000688812.1:c.1883C>T	ENSP00000510658.1:p.Ala628Val
ENST00000690544.1:c.*1178C>T	ENSP00000508989.1:n.*1178C>T
ENST00000358913.10:c.1907C>T MANE Select	ENSP00000351790.5:p.Ala636Val
ENST00000354393.6:c.1082C>T	ENSP00000346369.2:p.Ala361Val
ENST00000358913.9:c.1907C>T	ENSP00000351790.5:p.Ala636Val
ENST00000540630.5:c.1907C>T	ENSP00000441668.2:p.Ala636Val
ENST00000613327.4:c.1025C>T	ENSP00000480757.1:p.Ala342Val
NM_001256267.1:c.1907C>T	NP_001243196.1:p.Ala636Val
NM_001256268.1:c.1025C>T	NP_001243197.1:p.Ala342Val
NM_032578.3:c.1907C>T , LRG_410t1:c.1907C>T	NP_115967.2:p.Ala636Val
NR_045662.3:n.1334C>T
NR_045663.3:n.2175C>T
XM_006718043.2:c.1961C>T	XP_006718106.1:p.Ala654Val
XM_011540292.1:c.1937C>T	XP_011538594.1:p.Ala646Val
XM_017016833.1:c.1985C>T	XP_016872322.1:p.Ala662Val
XM_017016834.2:c.1907C>T	XP_016872323.1:p.Ala636Val
XM_024448236.1:c.785C>T	XP_024304004.1:p.Ala262Val
NR_045662.4:n.1444C>T
NR_045663.4:n.2120C>T
NM_001256267.2:c.1907C>T	NP_001243196.1:p.Ala636Val
NM_001256268.2:c.1025C>T	NP_001243197.1:p.Ala342Val
NM_032578.4:c.1907C>T MANE Select	NP_115967.2:p.Ala636Val