Canonical Allele Identifier: CA376837646

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69925466T>G (hg19) ; chr10:g.68165709T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165709T>G , CM000672.2:g.68165709T>G	GRCh38
NC_000010.10:g.69925466T>G , CM000672.1:g.69925466T>G	GRCh37
NC_000010.9:g.69595472T>G	NCBI36
NG_032118.1:g.64593T>G , LRG_410:g.64593T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.666T>G	ENSP00000346369.2:p.Ile222Met
ENST00000373675.4:c.1491T>G	ENSP00000362779.4:p.Ile497Met
ENST00000540630.6:c.1545T>G	ENSP00000441668.3:p.Ile515Met
ENST00000613327.5:c.1491T>G	ENSP00000480757.2:p.Ile497Met
ENST00000687572.1:c.369T>G	ENSP00000510427.1:p.Ile123Met
ENST00000687705.1:c.*1740T>G	ENSP00000509639.1:n.*1740T>G
ENST00000688812.1:c.1467T>G	ENSP00000510658.1:p.Ile489Met
ENST00000689002.1:n.543T>G
ENST00000690544.1:c.*762T>G	ENSP00000508989.1:n.*762T>G
ENST00000358913.10:c.1491T>G MANE Select	ENSP00000351790.5:p.Ile497Met
ENST00000354393.6:c.666T>G	ENSP00000346369.2:p.Ile222Met
ENST00000358913.9:c.1491T>G	ENSP00000351790.5:p.Ile497Met
ENST00000540630.5:c.1491T>G	ENSP00000441668.2:p.Ile497Met
ENST00000613327.4:c.609T>G	ENSP00000480757.1:p.Ile203Met
NM_001256267.1:c.1491T>G	NP_001243196.1:p.Ile497Met
NM_001256268.1:c.609T>G	NP_001243197.1:p.Ile203Met
NM_032578.3:c.1491T>G , LRG_410t1:c.1491T>G	NP_115967.2:p.Ile497Met
NR_045662.3:n.918T>G
NR_045663.3:n.1759T>G
XM_006718043.2:c.1545T>G	XP_006718106.1:p.Ile515Met
XM_011540292.1:c.1521T>G	XP_011538594.1:p.Ile507Met
XM_017016833.1:c.1569T>G	XP_016872322.1:p.Ile523Met
XM_017016834.2:c.1491T>G	XP_016872323.1:p.Ile497Met
XM_024448236.1:c.369T>G	XP_024304004.1:p.Ile123Met
NR_045662.4:n.1028T>G
NR_045663.4:n.1704T>G
NM_001256267.2:c.1491T>G	NP_001243196.1:p.Ile497Met
NM_001256268.2:c.609T>G	NP_001243197.1:p.Ile203Met
NM_032578.4:c.1491T>G MANE Select	NP_115967.2:p.Ile497Met