Canonical Allele Identifier: CA376841087

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926408T>A (hg19) ; chr10:g.68166651T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166651T>A , CM000672.2:g.68166651T>A	GRCh38
NC_000010.10:g.69926408T>A , CM000672.1:g.69926408T>A	GRCh37
NC_000010.9:g.69596414T>A	NCBI36
NG_032118.1:g.65535T>A , LRG_410:g.65535T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1133T>A	ENSP00000346369.2:p.Leu378Gln
ENST00000373675.4:c.1958T>A	ENSP00000362779.4:p.Leu653Gln
ENST00000540630.6:c.2012T>A	ENSP00000441668.3:p.Leu671Gln
ENST00000613327.5:c.1958T>A	ENSP00000480757.2:p.Leu653Gln
ENST00000687572.1:c.836T>A	ENSP00000510427.1:p.Leu279Gln
ENST00000688812.1:c.1934T>A	ENSP00000510658.1:p.Leu645Gln
ENST00000690544.1:c.*1229T>A	ENSP00000508989.1:n.*1229T>A
ENST00000358913.10:c.1958T>A MANE Select	ENSP00000351790.5:p.Leu653Gln
ENST00000354393.6:c.1133T>A	ENSP00000346369.2:p.Leu378Gln
ENST00000358913.9:c.1958T>A	ENSP00000351790.5:p.Leu653Gln
ENST00000540630.5:c.1958T>A	ENSP00000441668.2:p.Leu653Gln
ENST00000613327.4:c.1076T>A	ENSP00000480757.1:p.Leu359Gln
NM_001256267.1:c.1958T>A	NP_001243196.1:p.Leu653Gln
NM_001256268.1:c.1076T>A	NP_001243197.1:p.Leu359Gln
NM_032578.3:c.1958T>A , LRG_410t1:c.1958T>A	NP_115967.2:p.Leu653Gln
NR_045662.3:n.1385T>A
NR_045663.3:n.2226T>A
XM_006718043.2:c.2012T>A	XP_006718106.1:p.Leu671Gln
XM_011540292.1:c.1988T>A	XP_011538594.1:p.Leu663Gln
XM_017016833.1:c.2036T>A	XP_016872322.1:p.Leu679Gln
XM_017016834.2:c.1958T>A	XP_016872323.1:p.Leu653Gln
XM_024448236.1:c.836T>A	XP_024304004.1:p.Leu279Gln
NR_045662.4:n.1495T>A
NR_045663.4:n.2171T>A
NM_001256267.2:c.1958T>A	NP_001243196.1:p.Leu653Gln
NM_001256268.2:c.1076T>A	NP_001243197.1:p.Leu359Gln
NM_032578.4:c.1958T>A MANE Select	NP_115967.2:p.Leu653Gln