Canonical Allele Identifier: CA376858957

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69959155T>G (hg19) ; chr10:g.68199398T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199398T>G , CM000672.2:g.68199398T>G	GRCh38
NC_000010.10:g.69959155T>G , CM000672.1:g.69959155T>G	GRCh37
NC_000010.9:g.69629161T>G	NCBI36
NG_032118.1:g.98282T>G , LRG_410:g.98282T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2491T>G	ENSP00000346369.2:p.Trp831Gly
ENST00000540630.6:c.3370T>G	ENSP00000441668.3:p.Trp1124Gly
ENST00000613327.5:c.3316T>G	ENSP00000480757.2:p.Trp1106Gly
ENST00000688812.1:c.*579T>G	ENSP00000510658.1:n.*579T>G
ENST00000690544.1:c.*2587T>G	ENSP00000508989.1:n.*2587T>G
ENST00000358913.10:c.3316T>G MANE Select	ENSP00000351790.5:p.Trp1106Gly
ENST00000354393.6:c.2491T>G	ENSP00000346369.2:p.Trp831Gly
ENST00000358913.9:c.3316T>G	ENSP00000351790.5:p.Trp1106Gly
ENST00000540630.5:c.3316T>G	ENSP00000441668.2:p.Trp1106Gly
ENST00000613327.4:c.2434T>G	ENSP00000480757.1:p.Trp812Gly
NM_001256267.1:c.3316T>G	NP_001243196.1:p.Trp1106Gly
NM_001256268.1:c.2434T>G	NP_001243197.1:p.Trp812Gly
NM_032578.3:c.3316T>G , LRG_410t1:c.3316T>G	NP_115967.2:p.Trp1106Gly
NR_045662.3:n.2743T>G
NR_045663.3:n.3445T>G
XM_006718043.2:c.3370T>G	XP_006718106.1:p.Trp1124Gly
XM_011540292.1:c.3346T>G	XP_011538594.1:p.Trp1116Gly
XR_946029.1:n.1804-123A>C
XM_017016833.1:c.3394T>G	XP_016872322.1:p.Trp1132Gly
XM_017016834.2:c.3316T>G	XP_016872323.1:p.Trp1106Gly
XM_024448236.1:c.2194T>G	XP_024304004.1:p.Trp732Gly
NR_045662.4:n.2853T>G
NR_045663.4:n.3390T>G
NM_001256267.2:c.3316T>G	NP_001243196.1:p.Trp1106Gly
NM_001256268.2:c.2434T>G	NP_001243197.1:p.Trp812Gly
NM_032578.4:c.3316T>G MANE Select	NP_115967.2:p.Trp1106Gly