Canonical Allele Identifier: CA376837650

Gene: MYPN

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000354393.7:c.668G>A	ENSP00000346369.2:p.Cys223Tyr
ENST00000373675.4:c.1493G>A	ENSP00000362779.4:p.Cys498Tyr
ENST00000540630.6:c.1547G>A	ENSP00000441668.3:p.Cys516Tyr
ENST00000613327.5:c.1493G>A	ENSP00000480757.2:p.Cys498Tyr
ENST00000687572.1:c.371G>A	ENSP00000510427.1:p.Cys124Tyr
ENST00000687705.1:c.*1742G>A	ENSP00000509639.1:n.*1742G>A
ENST00000688812.1:c.1469G>A	ENSP00000510658.1:p.Cys490Tyr
ENST00000689002.1:n.545G>A
ENST00000690544.1:c.*764G>A	ENSP00000508989.1:n.*764G>A
ENST00000358913.10:c.1493G>A MANE Select	ENSP00000351790.5:p.Cys498Tyr
ENST00000354393.6:c.668G>A	ENSP00000346369.2:p.Cys223Tyr
ENST00000358913.9:c.1493G>A	ENSP00000351790.5:p.Cys498Tyr
ENST00000540630.5:c.1493G>A	ENSP00000441668.2:p.Cys498Tyr
ENST00000613327.4:c.611G>A	ENSP00000480757.1:p.Cys204Tyr
NM_001256267.1:c.1493G>A	NP_001243196.1:p.Cys498Tyr
NM_001256268.1:c.611G>A	NP_001243197.1:p.Cys204Tyr
NM_032578.3:c.1493G>A , LRG_410t1:c.1493G>A	NP_115967.2:p.Cys498Tyr
NR_045662.3:n.920G>A
NR_045663.3:n.1761G>A
XM_006718043.2:c.1547G>A	XP_006718106.1:p.Cys516Tyr
XM_011540292.1:c.1523G>A	XP_011538594.1:p.Cys508Tyr
XM_017016833.1:c.1571G>A	XP_016872322.1:p.Cys524Tyr
XM_017016834.2:c.1493G>A	XP_016872323.1:p.Cys498Tyr
XM_024448236.1:c.371G>A	XP_024304004.1:p.Cys124Tyr
NR_045662.4:n.1030G>A
NR_045663.4:n.1706G>A
NM_001256267.2:c.1493G>A	NP_001243196.1:p.Cys498Tyr
NM_001256268.2:c.611G>A	NP_001243197.1:p.Cys204Tyr
NM_032578.4:c.1493G>A MANE Select	NP_115967.2:p.Cys498Tyr