Canonical Allele Identifier: CA376839713

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926128C>G (hg19) ; chr10:g.68166371C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166371C>G , CM000672.2:g.68166371C>G	GRCh38
NC_000010.10:g.69926128C>G , CM000672.1:g.69926128C>G	GRCh37
NC_000010.9:g.69596134C>G	NCBI36
NG_032118.1:g.65255C>G , LRG_410:g.65255C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.853C>G	ENSP00000346369.2:p.Pro285Ala
ENST00000373675.4:c.1678C>G	ENSP00000362779.4:p.Pro560Ala
ENST00000540630.6:c.1732C>G	ENSP00000441668.3:p.Pro578Ala
ENST00000613327.5:c.1678C>G	ENSP00000480757.2:p.Pro560Ala
ENST00000687572.1:c.556C>G	ENSP00000510427.1:p.Pro186Ala
ENST00000687705.1:c.*1927C>G	ENSP00000509639.1:n.*1927C>G
ENST00000688812.1:c.1654C>G	ENSP00000510658.1:p.Pro552Ala
ENST00000689002.1:n.730C>G
ENST00000690544.1:c.*949C>G	ENSP00000508989.1:n.*949C>G
ENST00000358913.10:c.1678C>G MANE Select	ENSP00000351790.5:p.Pro560Ala
ENST00000354393.6:c.853C>G	ENSP00000346369.2:p.Pro285Ala
ENST00000358913.9:c.1678C>G	ENSP00000351790.5:p.Pro560Ala
ENST00000540630.5:c.1678C>G	ENSP00000441668.2:p.Pro560Ala
ENST00000613327.4:c.796C>G	ENSP00000480757.1:p.Pro266Ala
NM_001256267.1:c.1678C>G	NP_001243196.1:p.Pro560Ala
NM_001256268.1:c.796C>G	NP_001243197.1:p.Pro266Ala
NM_032578.3:c.1678C>G , LRG_410t1:c.1678C>G	NP_115967.2:p.Pro560Ala
NR_045662.3:n.1105C>G
NR_045663.3:n.1946C>G
XM_006718043.2:c.1732C>G	XP_006718106.1:p.Pro578Ala
XM_011540292.1:c.1708C>G	XP_011538594.1:p.Pro570Ala
XM_017016833.1:c.1756C>G	XP_016872322.1:p.Pro586Ala
XM_017016834.2:c.1678C>G	XP_016872323.1:p.Pro560Ala
XM_024448236.1:c.556C>G	XP_024304004.1:p.Pro186Ala
NR_045662.4:n.1215C>G
NR_045663.4:n.1891C>G
NM_001256267.2:c.1678C>G	NP_001243196.1:p.Pro560Ala
NM_001256268.2:c.796C>G	NP_001243197.1:p.Pro266Ala
NM_032578.4:c.1678C>G MANE Select	NP_115967.2:p.Pro560Ala