Canonical Allele Identifier: CA2573145232

Gene: MYPN

Linked Data

• ClinVar Variation Id: 1374949
• ClinVar RCV Id: RCV001879410
• dbSNP Id: rs2134169413

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166603dup , CM000672.2:g.68166603dup	GRCh38
NC_000010.10:g.69926360dup , CM000672.1:g.69926360dup	GRCh37
NC_000010.9:g.69596366dup	NCBI36
NG_032118.1:g.65487dup , LRG_410:g.65487dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1085dup	ENSP00000346369.2:p.Thr364AsnfsTer21
ENST00000373675.4:c.1910dup	ENSP00000362779.4:p.Thr639AsnfsTer25
ENST00000540630.6:c.1964dup	ENSP00000441668.3:p.Thr657AsnfsTer21
ENST00000613327.5:c.1910dup	ENSP00000480757.2:p.Thr639AsnfsTer21
ENST00000687572.1:c.788dup	ENSP00000510427.1:p.Thr265AsnfsTer?
ENST00000688812.1:c.1886dup	ENSP00000510658.1:p.Thr631AsnfsTer21
ENST00000690544.1:c.*1181dup	ENSP00000508989.1:n.*1181dup
ENST00000358913.10:c.1910dup MANE Select	ENSP00000351790.5:p.Thr639AsnfsTer21
ENST00000354393.6:c.1085dup	ENSP00000346369.2:p.Thr364AsnfsTer21
ENST00000358913.9:c.1910dup	ENSP00000351790.5:p.Thr639AsnfsTer21
ENST00000540630.5:c.1910dup	ENSP00000441668.2:p.Thr639AsnfsTer21
ENST00000613327.4:c.1028dup	ENSP00000480757.1:p.Thr345AsnfsTer21
NM_001256267.1:c.1910dup	NP_001243196.1:p.Thr639AsnfsTer21
NM_001256268.1:c.1028dup	NP_001243197.1:p.Thr345AsnfsTer21
NM_032578.3:c.1910dup , LRG_410t1:c.1910dup	NP_115967.2:p.Thr639AsnfsTer21
NR_045662.3:n.1337dup
NR_045663.3:n.2178dup
XM_006718043.2:c.1964dup	XP_006718106.1:p.Thr657AsnfsTer21
XM_011540292.1:c.1940dup	XP_011538594.1:p.Thr649AsnfsTer21
XM_017016833.1:c.1988dup	XP_016872322.1:p.Thr665AsnfsTer21
XM_017016834.2:c.1910dup	XP_016872323.1:p.Thr639AsnfsTer21
XM_024448236.1:c.788dup	XP_024304004.1:p.Thr265AsnfsTer21
NR_045662.4:n.1447dup
NR_045663.4:n.2123dup
NM_001256267.2:c.1910dup	NP_001243196.1:p.Thr639AsnfsTer21
NM_001256268.2:c.1028dup	NP_001243197.1:p.Thr345AsnfsTer21
NM_032578.4:c.1910dup MANE Select	NP_115967.2:p.Thr639AsnfsTer21