Canonical Allele Identifier: CA376837658

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69925468G>T (hg19) ; chr10:g.68165711G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165711G>T , CM000672.2:g.68165711G>T	GRCh38
NC_000010.10:g.69925468G>T , CM000672.1:g.69925468G>T	GRCh37
NC_000010.9:g.69595474G>T	NCBI36
NG_032118.1:g.64595G>T , LRG_410:g.64595G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000354393.7:c.668G>T	ENSP00000346369.2:p.Cys223Phe
ENST00000373675.4:c.1493G>T	ENSP00000362779.4:p.Cys498Phe
ENST00000540630.6:c.1547G>T	ENSP00000441668.3:p.Cys516Phe
ENST00000613327.5:c.1493G>T	ENSP00000480757.2:p.Cys498Phe
ENST00000687572.1:c.371G>T	ENSP00000510427.1:p.Cys124Phe
ENST00000687705.1:c.*1742G>T	ENSP00000509639.1:n.*1742G>T
ENST00000688812.1:c.1469G>T	ENSP00000510658.1:p.Cys490Phe
ENST00000689002.1:n.545G>T
ENST00000690544.1:c.*764G>T	ENSP00000508989.1:n.*764G>T
ENST00000358913.10:c.1493G>T MANE Select	ENSP00000351790.5:p.Cys498Phe
ENST00000354393.6:c.668G>T	ENSP00000346369.2:p.Cys223Phe
ENST00000358913.9:c.1493G>T	ENSP00000351790.5:p.Cys498Phe
ENST00000540630.5:c.1493G>T	ENSP00000441668.2:p.Cys498Phe
ENST00000613327.4:c.611G>T	ENSP00000480757.1:p.Cys204Phe
NM_001256267.1:c.1493G>T	NP_001243196.1:p.Cys498Phe
NM_001256268.1:c.611G>T	NP_001243197.1:p.Cys204Phe
NM_032578.3:c.1493G>T , LRG_410t1:c.1493G>T	NP_115967.2:p.Cys498Phe
NR_045662.3:n.920G>T
NR_045663.3:n.1761G>T
XM_006718043.2:c.1547G>T	XP_006718106.1:p.Cys516Phe
XM_011540292.1:c.1523G>T	XP_011538594.1:p.Cys508Phe
XM_017016833.1:c.1571G>T	XP_016872322.1:p.Cys524Phe
XM_017016834.2:c.1493G>T	XP_016872323.1:p.Cys498Phe
XM_024448236.1:c.371G>T	XP_024304004.1:p.Cys124Phe
NR_045662.4:n.1030G>T
NR_045663.4:n.1706G>T
NM_001256267.2:c.1493G>T	NP_001243196.1:p.Cys498Phe
NM_001256268.2:c.611G>T	NP_001243197.1:p.Cys204Phe
NM_032578.4:c.1493G>T MANE Select	NP_115967.2:p.Cys498Phe