Canonical Allele Identifier: CA469805686

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926112A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166355A>G , CM000672.2:g.68166355A>G	GRCh38
NC_000010.10:g.69926112A>G , CM000672.1:g.69926112A>G	GRCh37
NC_000010.9:g.69596118A>G	NCBI36
NG_032118.1:g.65239A>G , LRG_410:g.65239A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.837A>G	ENSP00000346369.2:p.Ala279=
ENST00000373675.4:c.1662A>G	ENSP00000362779.4:p.Ala554=
ENST00000540630.6:c.1716A>G	ENSP00000441668.3:p.Ala572=
ENST00000613327.5:c.1662A>G	ENSP00000480757.2:p.Ala554=
ENST00000687572.1:c.540A>G	ENSP00000510427.1:p.Ala180=
ENST00000687705.1:c.*1911A>G	ENSP00000509639.1:n.*1911A>G
ENST00000688812.1:c.1638A>G	ENSP00000510658.1:p.Ala546=
ENST00000689002.1:n.714A>G
ENST00000690544.1:c.*933A>G	ENSP00000508989.1:n.*933A>G
ENST00000358913.10:c.1662A>G MANE Select	ENSP00000351790.5:p.Ala554=
ENST00000354393.6:c.837A>G	ENSP00000346369.2:p.Ala279=
ENST00000358913.9:c.1662A>G	ENSP00000351790.5:p.Ala554=
ENST00000540630.5:c.1662A>G	ENSP00000441668.2:p.Ala554=
ENST00000613327.4:c.780A>G	ENSP00000480757.1:p.Ala260=
NM_001256267.1:c.1662A>G	NP_001243196.1:p.Ala554=
NM_001256268.1:c.780A>G	NP_001243197.1:p.Ala260=
NM_032578.3:c.1662A>G , LRG_410t1:c.1662A>G	NP_115967.2:p.Ala554=
NR_045662.3:n.1089A>G
NR_045663.3:n.1930A>G
XM_006718043.2:c.1716A>G	XP_006718106.1:p.Ala572=
XM_011540292.1:c.1692A>G	XP_011538594.1:p.Ala564=
XM_017016833.1:c.1740A>G	XP_016872322.1:p.Ala580=
XM_017016834.2:c.1662A>G	XP_016872323.1:p.Ala554=
XM_024448236.1:c.540A>G	XP_024304004.1:p.Ala180=
NR_045662.4:n.1199A>G
NR_045663.4:n.1875A>G
NM_001256267.2:c.1662A>G	NP_001243196.1:p.Ala554=
NM_001256268.2:c.780A>G	NP_001243197.1:p.Ala260=
NM_032578.4:c.1662A>G MANE Select	NP_115967.2:p.Ala554=