Canonical Allele Identifier: CA376859217

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69959231T>A (hg19) ; chr10:g.68199474T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199474T>A , CM000672.2:g.68199474T>A	GRCh38
NC_000010.10:g.69959231T>A , CM000672.1:g.69959231T>A	GRCh37
NC_000010.9:g.69629237T>A	NCBI36
NG_032118.1:g.98358T>A , LRG_410:g.98358T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2567T>A	ENSP00000346369.2:p.Leu856Gln
ENST00000540630.6:c.3446T>A	ENSP00000441668.3:p.Leu1149Gln
ENST00000613327.5:c.3392T>A	ENSP00000480757.2:p.Leu1131Gln
ENST00000688812.1:c.*655T>A	ENSP00000510658.1:n.*655T>A
ENST00000690544.1:c.*2663T>A	ENSP00000508989.1:n.*2663T>A
ENST00000358913.10:c.3392T>A MANE Select	ENSP00000351790.5:p.Leu1131Gln
ENST00000354393.6:c.2567T>A	ENSP00000346369.2:p.Leu856Gln
ENST00000358913.9:c.3392T>A	ENSP00000351790.5:p.Leu1131Gln
ENST00000540630.5:c.3392T>A	ENSP00000441668.2:p.Leu1131Gln
ENST00000613327.4:c.2510T>A	ENSP00000480757.1:p.Leu837Gln
NM_001256267.1:c.3392T>A	NP_001243196.1:p.Leu1131Gln
NM_001256268.1:c.2510T>A	NP_001243197.1:p.Leu837Gln
NM_032578.3:c.3392T>A , LRG_410t1:c.3392T>A	NP_115967.2:p.Leu1131Gln
NR_045662.3:n.2819T>A
NR_045663.3:n.3521T>A
XM_006718043.2:c.3446T>A	XP_006718106.1:p.Leu1149Gln
XM_011540292.1:c.3422T>A	XP_011538594.1:p.Leu1141Gln
XR_946029.1:n.1804-199A>T
XM_017016833.1:c.3470T>A	XP_016872322.1:p.Leu1157Gln
XM_017016834.2:c.3392T>A	XP_016872323.1:p.Leu1131Gln
XM_024448236.1:c.2270T>A	XP_024304004.1:p.Leu757Gln
NR_045662.4:n.2929T>A
NR_045663.4:n.3466T>A
NM_001256267.2:c.3392T>A	NP_001243196.1:p.Leu1131Gln
NM_001256268.2:c.2510T>A	NP_001243197.1:p.Leu837Gln
NM_032578.4:c.3392T>A MANE Select	NP_115967.2:p.Leu1131Gln