Canonical Allele Identifier: CA376839886

Gene: MYPN

Linked Data

• ClinVar Variation Id: 2563968
• ClinVar RCV Id: RCV003306297
• MyVariant Identifiers: chr10:g.69926167C>G (hg19) ; chr10:g.68166410C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166410C>G , CM000672.2:g.68166410C>G	GRCh38
NC_000010.10:g.69926167C>G , CM000672.1:g.69926167C>G	GRCh37
NC_000010.9:g.69596173C>G	NCBI36
NG_032118.1:g.65294C>G , LRG_410:g.65294C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.892C>G	ENSP00000346369.2:p.Pro298Ala
ENST00000373675.4:c.1717C>G	ENSP00000362779.4:p.Pro573Ala
ENST00000540630.6:c.1771C>G	ENSP00000441668.3:p.Pro591Ala
ENST00000613327.5:c.1717C>G	ENSP00000480757.2:p.Pro573Ala
ENST00000687572.1:c.595C>G	ENSP00000510427.1:p.Pro199Ala
ENST00000688812.1:c.1693C>G	ENSP00000510658.1:p.Pro565Ala
ENST00000689002.1:n.769C>G
ENST00000690544.1:c.*988C>G	ENSP00000508989.1:n.*988C>G
ENST00000358913.10:c.1717C>G MANE Select	ENSP00000351790.5:p.Pro573Ala
ENST00000354393.6:c.892C>G	ENSP00000346369.2:p.Pro298Ala
ENST00000358913.9:c.1717C>G	ENSP00000351790.5:p.Pro573Ala
ENST00000540630.5:c.1717C>G	ENSP00000441668.2:p.Pro573Ala
ENST00000613327.4:c.835C>G	ENSP00000480757.1:p.Pro279Ala
NM_001256267.1:c.1717C>G	NP_001243196.1:p.Pro573Ala
NM_001256268.1:c.835C>G	NP_001243197.1:p.Pro279Ala
NM_032578.3:c.1717C>G , LRG_410t1:c.1717C>G	NP_115967.2:p.Pro573Ala
NR_045662.3:n.1144C>G
NR_045663.3:n.1985C>G
XM_006718043.2:c.1771C>G	XP_006718106.1:p.Pro591Ala
XM_011540292.1:c.1747C>G	XP_011538594.1:p.Pro583Ala
XM_017016833.1:c.1795C>G	XP_016872322.1:p.Pro599Ala
XM_017016834.2:c.1717C>G	XP_016872323.1:p.Pro573Ala
XM_024448236.1:c.595C>G	XP_024304004.1:p.Pro199Ala
NR_045662.4:n.1254C>G
NR_045663.4:n.1930C>G
NM_001256267.2:c.1717C>G	NP_001243196.1:p.Pro573Ala
NM_001256268.2:c.835C>G	NP_001243197.1:p.Pro279Ala
NM_032578.4:c.1717C>G MANE Select	NP_115967.2:p.Pro573Ala