Canonical Allele Identifier: CA376839760

Gene: MYPN

Linked Data

• gnomAD v4: 10-68166381-C-G
• MyVariant Identifiers: chr10:g.69926138C>G (hg19) ; chr10:g.68166381C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166381C>G , CM000672.2:g.68166381C>G	GRCh38
NC_000010.10:g.69926138C>G , CM000672.1:g.69926138C>G	GRCh37
NC_000010.9:g.69596144C>G	NCBI36
NG_032118.1:g.65265C>G , LRG_410:g.65265C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.863C>G	ENSP00000346369.2:p.Pro288Arg
ENST00000373675.4:c.1688C>G	ENSP00000362779.4:p.Pro563Arg
ENST00000540630.6:c.1742C>G	ENSP00000441668.3:p.Pro581Arg
ENST00000613327.5:c.1688C>G	ENSP00000480757.2:p.Pro563Arg
ENST00000687572.1:c.566C>G	ENSP00000510427.1:p.Pro189Arg
ENST00000688812.1:c.1664C>G	ENSP00000510658.1:p.Pro555Arg
ENST00000689002.1:n.740C>G
ENST00000690544.1:c.*959C>G	ENSP00000508989.1:n.*959C>G
ENST00000358913.10:c.1688C>G MANE Select	ENSP00000351790.5:p.Pro563Arg
ENST00000354393.6:c.863C>G	ENSP00000346369.2:p.Pro288Arg
ENST00000358913.9:c.1688C>G	ENSP00000351790.5:p.Pro563Arg
ENST00000540630.5:c.1688C>G	ENSP00000441668.2:p.Pro563Arg
ENST00000613327.4:c.806C>G	ENSP00000480757.1:p.Pro269Arg
NM_001256267.1:c.1688C>G	NP_001243196.1:p.Pro563Arg
NM_001256268.1:c.806C>G	NP_001243197.1:p.Pro269Arg
NM_032578.3:c.1688C>G , LRG_410t1:c.1688C>G	NP_115967.2:p.Pro563Arg
NR_045662.3:n.1115C>G
NR_045663.3:n.1956C>G
XM_006718043.2:c.1742C>G	XP_006718106.1:p.Pro581Arg
XM_011540292.1:c.1718C>G	XP_011538594.1:p.Pro573Arg
XM_017016833.1:c.1766C>G	XP_016872322.1:p.Pro589Arg
XM_017016834.2:c.1688C>G	XP_016872323.1:p.Pro563Arg
XM_024448236.1:c.566C>G	XP_024304004.1:p.Pro189Arg
NR_045662.4:n.1225C>G
NR_045663.4:n.1901C>G
NM_001256267.2:c.1688C>G	NP_001243196.1:p.Pro563Arg
NM_001256268.2:c.806C>G	NP_001243197.1:p.Pro269Arg
NM_032578.4:c.1688C>G MANE Select	NP_115967.2:p.Pro563Arg