Canonical Allele Identifier: CA376839898

Gene: MYPN

Linked Data

• ClinVar Variation Id: 1955577
• ClinVar RCV Id: RCV002695495
• dbSNP Id: rs1227712777
• gnomAD v2: 10-69926170-C-G
• gnomAD v4: 10-68166413-C-G
• MyVariant Identifiers: chr10:g.69926170C>G (hg19) ; chr10:g.68166413C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166413C>G , CM000672.2:g.68166413C>G	GRCh38
NC_000010.10:g.69926170C>G , CM000672.1:g.69926170C>G	GRCh37
NC_000010.9:g.69596176C>G	NCBI36
NG_032118.1:g.65297C>G , LRG_410:g.65297C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.895C>G	ENSP00000346369.2:p.Pro299Ala
ENST00000373675.4:c.1720C>G	ENSP00000362779.4:p.Pro574Ala
ENST00000540630.6:c.1774C>G	ENSP00000441668.3:p.Pro592Ala
ENST00000613327.5:c.1720C>G	ENSP00000480757.2:p.Pro574Ala
ENST00000687572.1:c.598C>G	ENSP00000510427.1:p.Pro200Ala
ENST00000688812.1:c.1696C>G	ENSP00000510658.1:p.Pro566Ala
ENST00000689002.1:n.772C>G
ENST00000690544.1:c.*991C>G	ENSP00000508989.1:n.*991C>G
ENST00000358913.10:c.1720C>G MANE Select	ENSP00000351790.5:p.Pro574Ala
ENST00000354393.6:c.895C>G	ENSP00000346369.2:p.Pro299Ala
ENST00000358913.9:c.1720C>G	ENSP00000351790.5:p.Pro574Ala
ENST00000540630.5:c.1720C>G	ENSP00000441668.2:p.Pro574Ala
ENST00000613327.4:c.838C>G	ENSP00000480757.1:p.Pro280Ala
NM_001256267.1:c.1720C>G	NP_001243196.1:p.Pro574Ala
NM_001256268.1:c.838C>G	NP_001243197.1:p.Pro280Ala
NM_032578.3:c.1720C>G , LRG_410t1:c.1720C>G	NP_115967.2:p.Pro574Ala
NR_045662.3:n.1147C>G
NR_045663.3:n.1988C>G
XM_006718043.2:c.1774C>G	XP_006718106.1:p.Pro592Ala
XM_011540292.1:c.1750C>G	XP_011538594.1:p.Pro584Ala
XM_017016833.1:c.1798C>G	XP_016872322.1:p.Pro600Ala
XM_017016834.2:c.1720C>G	XP_016872323.1:p.Pro574Ala
XM_024448236.1:c.598C>G	XP_024304004.1:p.Pro200Ala
NR_045662.4:n.1257C>G
NR_045663.4:n.1933C>G
NM_001256267.2:c.1720C>G	NP_001243196.1:p.Pro574Ala
NM_001256268.2:c.838C>G	NP_001243197.1:p.Pro280Ala
NM_032578.4:c.1720C>G MANE Select	NP_115967.2:p.Pro574Ala