Canonical Allele Identifier: CA5522677

Gene: MYPN

Linked Data

• dbSNP Id: rs752536783
• ExAC: 10:69926345 T / G
• gnomAD v2: 10-69926345-T-G
• gnomAD v4: 10-68166588-T-G
• MyVariant Identifiers: chr10:g.69926345T>G (hg19) ; chr10:g.68166588T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166588T>G , CM000672.2:g.68166588T>G	GRCh38
NC_000010.10:g.69926345T>G , CM000672.1:g.69926345T>G	GRCh37
NC_000010.9:g.69596351T>G	NCBI36
NG_032118.1:g.65472T>G , LRG_410:g.65472T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1070T>G	ENSP00000346369.2:p.Phe357Cys
ENST00000373675.4:c.1895T>G	ENSP00000362779.4:p.Phe632Cys
ENST00000540630.6:c.1949T>G	ENSP00000441668.3:p.Phe650Cys
ENST00000613327.5:c.1895T>G	ENSP00000480757.2:p.Phe632Cys
ENST00000687572.1:c.773T>G	ENSP00000510427.1:p.Phe258Cys
ENST00000688812.1:c.1871T>G	ENSP00000510658.1:p.Phe624Cys
ENST00000690544.1:c.*1166T>G	ENSP00000508989.1:n.*1166T>G
ENST00000358913.10:c.1895T>G MANE Select	ENSP00000351790.5:p.Phe632Cys
ENST00000354393.6:c.1070T>G	ENSP00000346369.2:p.Phe357Cys
ENST00000358913.9:c.1895T>G	ENSP00000351790.5:p.Phe632Cys
ENST00000540630.5:c.1895T>G	ENSP00000441668.2:p.Phe632Cys
ENST00000613327.4:c.1013T>G	ENSP00000480757.1:p.Phe338Cys
NM_001256267.1:c.1895T>G	NP_001243196.1:p.Phe632Cys
NM_001256268.1:c.1013T>G	NP_001243197.1:p.Phe338Cys
NM_032578.3:c.1895T>G , LRG_410t1:c.1895T>G	NP_115967.2:p.Phe632Cys
NR_045662.3:n.1322T>G
NR_045663.3:n.2163T>G
XM_006718043.2:c.1949T>G	XP_006718106.1:p.Phe650Cys
XM_011540292.1:c.1925T>G	XP_011538594.1:p.Phe642Cys
XM_017016833.1:c.1973T>G	XP_016872322.1:p.Phe658Cys
XM_017016834.2:c.1895T>G	XP_016872323.1:p.Phe632Cys
XM_024448236.1:c.773T>G	XP_024304004.1:p.Phe258Cys
NR_045662.4:n.1432T>G
NR_045663.4:n.2108T>G
NM_001256267.2:c.1895T>G	NP_001243196.1:p.Phe632Cys
NM_001256268.2:c.1013T>G	NP_001243197.1:p.Phe338Cys
NM_032578.4:c.1895T>G MANE Select	NP_115967.2:p.Phe632Cys