Canonical Allele Identifier: CA376840930

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926383C>A (hg19) ; chr10:g.68166626C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166626C>A , CM000672.2:g.68166626C>A	GRCh38
NC_000010.10:g.69926383C>A , CM000672.1:g.69926383C>A	GRCh37
NC_000010.9:g.69596389C>A	NCBI36
NG_032118.1:g.65510C>A , LRG_410:g.65510C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1108C>A	ENSP00000346369.2:p.Pro370Thr
ENST00000373675.4:c.1933C>A	ENSP00000362779.4:p.Pro645Thr
ENST00000540630.6:c.1987C>A	ENSP00000441668.3:p.Pro663Thr
ENST00000613327.5:c.1933C>A	ENSP00000480757.2:p.Pro645Thr
ENST00000687572.1:c.811C>A	ENSP00000510427.1:p.Pro271Thr
ENST00000688812.1:c.1909C>A	ENSP00000510658.1:p.Pro637Thr
ENST00000690544.1:c.*1204C>A	ENSP00000508989.1:n.*1204C>A
ENST00000358913.10:c.1933C>A MANE Select	ENSP00000351790.5:p.Pro645Thr
ENST00000354393.6:c.1108C>A	ENSP00000346369.2:p.Pro370Thr
ENST00000358913.9:c.1933C>A	ENSP00000351790.5:p.Pro645Thr
ENST00000540630.5:c.1933C>A	ENSP00000441668.2:p.Pro645Thr
ENST00000613327.4:c.1051C>A	ENSP00000480757.1:p.Pro351Thr
NM_001256267.1:c.1933C>A	NP_001243196.1:p.Pro645Thr
NM_001256268.1:c.1051C>A	NP_001243197.1:p.Pro351Thr
NM_032578.3:c.1933C>A , LRG_410t1:c.1933C>A	NP_115967.2:p.Pro645Thr
NR_045662.3:n.1360C>A
NR_045663.3:n.2201C>A
XM_006718043.2:c.1987C>A	XP_006718106.1:p.Pro663Thr
XM_011540292.1:c.1963C>A	XP_011538594.1:p.Pro655Thr
XM_017016833.1:c.2011C>A	XP_016872322.1:p.Pro671Thr
XM_017016834.2:c.1933C>A	XP_016872323.1:p.Pro645Thr
XM_024448236.1:c.811C>A	XP_024304004.1:p.Pro271Thr
NR_045662.4:n.1470C>A
NR_045663.4:n.2146C>A
NM_001256267.2:c.1933C>A	NP_001243196.1:p.Pro645Thr
NM_001256268.2:c.1051C>A	NP_001243197.1:p.Pro351Thr
NM_032578.4:c.1933C>A MANE Select	NP_115967.2:p.Pro645Thr