Canonical Allele Identifier: CA376858885

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199378T>G , CM000672.2:g.68199378T>G	GRCh38
NC_000010.10:g.69959135T>G , CM000672.1:g.69959135T>G	GRCh37
NC_000010.9:g.69629141T>G	NCBI36
NG_032118.1:g.98262T>G , LRG_410:g.98262T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3296T>G MANE Select	NP_115967.2:p.Leu1099Ter
ENST00000358913.10:c.3296T>G MANE Select	ENSP00000351790.5:p.Leu1099Ter
NM_001256267.1:c.3296T>G	NP_001243196.1:p.Leu1099Ter
NM_001256267.2:c.3296T>G	NP_001243196.1:p.Leu1099Ter
NM_001256268.1:c.2414T>G	NP_001243197.1:p.Leu805Ter
NM_001256268.2:c.2414T>G	NP_001243197.1:p.Leu805Ter
NM_032578.3:c.3296T>G , LRG_410t1:c.3296T>G	NP_115967.2:p.Leu1099Ter
NR_045662.3:n.2723T>G
NR_045662.4:n.2833T>G
NR_045663.3:n.3425T>G
NR_045663.4:n.3370T>G
ENST00000354393.6:c.2471T>G	ENSP00000346369.2:p.Leu824Ter
ENST00000354393.7:c.2471T>G	ENSP00000346369.2:p.Leu824Ter
ENST00000358913.9:c.3296T>G	ENSP00000351790.5:p.Leu1099Ter
ENST00000540630.5:c.3296T>G	ENSP00000441668.2:p.Leu1099Ter
ENST00000540630.6:c.3350T>G	ENSP00000441668.3:p.Leu1117Ter
ENST00000613327.4:c.2414T>G	ENSP00000480757.1:p.Leu805Ter
ENST00000613327.5:c.3296T>G	ENSP00000480757.2:p.Leu1099Ter
ENST00000688812.1:c.*559T>G	ENSP00000510658.1:n.*559T>G
ENST00000690544.1:c.*2567T>G	ENSP00000508989.1:n.*2567T>G
XM_006718043.2:c.3350T>G	XP_006718106.1:p.Leu1117Ter
XM_011540292.1:c.3326T>G	XP_011538594.1:p.Leu1109Ter
XM_017016833.1:c.3374T>G	XP_016872322.1:p.Leu1125Ter
XM_017016834.2:c.3296T>G	XP_016872323.1:p.Leu1099Ter
XM_024448236.1:c.2174T>G	XP_024304004.1:p.Leu725Ter
XR_946029.1:n.1804-103A>C