Canonical Allele Identifier: CA376840925

Gene: MYPN

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1108C>T	ENSP00000346369.2:p.Pro370Ser
ENST00000373675.4:c.1933C>T	ENSP00000362779.4:p.Pro645Ser
ENST00000540630.6:c.1987C>T	ENSP00000441668.3:p.Pro663Ser
ENST00000613327.5:c.1933C>T	ENSP00000480757.2:p.Pro645Ser
ENST00000687572.1:c.811C>T	ENSP00000510427.1:p.Pro271Ser
ENST00000688812.1:c.1909C>T	ENSP00000510658.1:p.Pro637Ser
ENST00000690544.1:c.*1204C>T	ENSP00000508989.1:n.*1204C>T
ENST00000358913.10:c.1933C>T MANE Select	ENSP00000351790.5:p.Pro645Ser
ENST00000354393.6:c.1108C>T	ENSP00000346369.2:p.Pro370Ser
ENST00000358913.9:c.1933C>T	ENSP00000351790.5:p.Pro645Ser
ENST00000540630.5:c.1933C>T	ENSP00000441668.2:p.Pro645Ser
ENST00000613327.4:c.1051C>T	ENSP00000480757.1:p.Pro351Ser
NM_001256267.1:c.1933C>T	NP_001243196.1:p.Pro645Ser
NM_001256268.1:c.1051C>T	NP_001243197.1:p.Pro351Ser
NM_032578.3:c.1933C>T , LRG_410t1:c.1933C>T	NP_115967.2:p.Pro645Ser
NR_045662.3:n.1360C>T
NR_045663.3:n.2201C>T
XM_006718043.2:c.1987C>T	XP_006718106.1:p.Pro663Ser
XM_011540292.1:c.1963C>T	XP_011538594.1:p.Pro655Ser
XM_017016833.1:c.2011C>T	XP_016872322.1:p.Pro671Ser
XM_017016834.2:c.1933C>T	XP_016872323.1:p.Pro645Ser
XM_024448236.1:c.811C>T	XP_024304004.1:p.Pro271Ser
NR_045662.4:n.1470C>T
NR_045663.4:n.2146C>T
NM_001256267.2:c.1933C>T	NP_001243196.1:p.Pro645Ser
NM_001256268.2:c.1051C>T	NP_001243197.1:p.Pro351Ser
NM_032578.4:c.1933C>T MANE Select	NP_115967.2:p.Pro645Ser