Canonical Allele Identifier: CA5522642

Gene: MYPN

Linked Data

• dbSNP Id: rs749347548
• ExAC: 10:69926150 C / G
• gnomAD v2: 10-69926150-C-G
• gnomAD v4: 10-68166393-C-G
• MyVariant Identifiers: chr10:g.69926150C>G (hg19) ; chr10:g.68166393C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166393C>G , CM000672.2:g.68166393C>G	GRCh38
NC_000010.10:g.69926150C>G , CM000672.1:g.69926150C>G	GRCh37
NC_000010.9:g.69596156C>G	NCBI36
NG_032118.1:g.65277C>G , LRG_410:g.65277C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.875C>G	ENSP00000346369.2:p.Pro292Arg
ENST00000373675.4:c.1700C>G	ENSP00000362779.4:p.Pro567Arg
ENST00000540630.6:c.1754C>G	ENSP00000441668.3:p.Pro585Arg
ENST00000613327.5:c.1700C>G	ENSP00000480757.2:p.Pro567Arg
ENST00000687572.1:c.578C>G	ENSP00000510427.1:p.Pro193Arg
ENST00000688812.1:c.1676C>G	ENSP00000510658.1:p.Pro559Arg
ENST00000689002.1:n.752C>G
ENST00000690544.1:c.*971C>G	ENSP00000508989.1:n.*971C>G
ENST00000358913.10:c.1700C>G MANE Select	ENSP00000351790.5:p.Pro567Arg
ENST00000354393.6:c.875C>G	ENSP00000346369.2:p.Pro292Arg
ENST00000358913.9:c.1700C>G	ENSP00000351790.5:p.Pro567Arg
ENST00000540630.5:c.1700C>G	ENSP00000441668.2:p.Pro567Arg
ENST00000613327.4:c.818C>G	ENSP00000480757.1:p.Pro273Arg
NM_001256267.1:c.1700C>G	NP_001243196.1:p.Pro567Arg
NM_001256268.1:c.818C>G	NP_001243197.1:p.Pro273Arg
NM_032578.3:c.1700C>G , LRG_410t1:c.1700C>G	NP_115967.2:p.Pro567Arg
NR_045662.3:n.1127C>G
NR_045663.3:n.1968C>G
XM_006718043.2:c.1754C>G	XP_006718106.1:p.Pro585Arg
XM_011540292.1:c.1730C>G	XP_011538594.1:p.Pro577Arg
XM_017016833.1:c.1778C>G	XP_016872322.1:p.Pro593Arg
XM_017016834.2:c.1700C>G	XP_016872323.1:p.Pro567Arg
XM_024448236.1:c.578C>G	XP_024304004.1:p.Pro193Arg
NR_045662.4:n.1237C>G
NR_045663.4:n.1913C>G
NM_001256267.2:c.1700C>G	NP_001243196.1:p.Pro567Arg
NM_001256268.2:c.818C>G	NP_001243197.1:p.Pro273Arg
NM_032578.4:c.1700C>G MANE Select	NP_115967.2:p.Pro567Arg