Canonical Allele Identifier: CA376857671

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69955274C>T (hg19) ; chr10:g.68195517C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195517C>T , CM000672.2:g.68195517C>T	GRCh38
NC_000010.10:g.69955274C>T , CM000672.1:g.69955274C>T	GRCh37
NC_000010.9:g.69625280C>T	NCBI36
NG_032118.1:g.94401C>T , LRG_410:g.94401C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2318C>T	ENSP00000346369.2:p.Ala773Val
ENST00000540630.6:c.3197C>T	ENSP00000441668.3:p.Ala1066Val
ENST00000613327.5:c.3143C>T	ENSP00000480757.2:p.Ala1048Val
ENST00000688812.1:c.*406C>T	ENSP00000510658.1:n.*406C>T
ENST00000690544.1:c.*2414C>T	ENSP00000508989.1:n.*2414C>T
ENST00000358913.10:c.3143C>T MANE Select	ENSP00000351790.5:p.Ala1048Val
ENST00000354393.6:c.2318C>T	ENSP00000346369.2:p.Ala773Val
ENST00000358913.9:c.3143C>T	ENSP00000351790.5:p.Ala1048Val
ENST00000540630.5:c.3143C>T	ENSP00000441668.2:p.Ala1048Val
ENST00000613327.4:c.2261C>T	ENSP00000480757.1:p.Ala754Val
NM_001256267.1:c.3143C>T	NP_001243196.1:p.Ala1048Val
NM_001256268.1:c.2261C>T	NP_001243197.1:p.Ala754Val
NM_032578.3:c.3143C>T , LRG_410t1:c.3143C>T	NP_115967.2:p.Ala1048Val
NR_045662.3:n.2570C>T
NR_045663.3:n.3272C>T
XM_006718043.2:c.3197C>T	XP_006718106.1:p.Ala1066Val
XM_011540292.1:c.3173C>T	XP_011538594.1:p.Ala1058Val
XM_017016833.1:c.3221C>T	XP_016872322.1:p.Ala1074Val
XM_017016834.2:c.3143C>T	XP_016872323.1:p.Ala1048Val
XM_024448236.1:c.2021C>T	XP_024304004.1:p.Ala674Val
NR_045662.4:n.2680C>T
NR_045663.4:n.3217C>T
NM_001256267.2:c.3143C>T	NP_001243196.1:p.Ala1048Val
NM_001256268.2:c.2261C>T	NP_001243197.1:p.Ala754Val
NM_032578.4:c.3143C>T MANE Select	NP_115967.2:p.Ala1048Val