Canonical Allele Identifier: CA469812985

Gene: MYPN

Linked Data

• COSMIC: COSM2159135 ; COSM4179665 ; COSM4179666
• MyVariant Identifiers: chr10:g.69926283A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166526A>T , CM000672.2:g.68166526A>T	GRCh38
NC_000010.10:g.69926283A>T , CM000672.1:g.69926283A>T	GRCh37
NC_000010.9:g.69596289A>T	NCBI36
NG_032118.1:g.65410A>T , LRG_410:g.65410A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1008A>T	ENSP00000346369.2:p.Ala336=
ENST00000373675.4:c.1833A>T	ENSP00000362779.4:p.Ala611=
ENST00000540630.6:c.1887A>T	ENSP00000441668.3:p.Ala629=
ENST00000613327.5:c.1833A>T	ENSP00000480757.2:p.Ala611=
ENST00000687572.1:c.711A>T	ENSP00000510427.1:p.Ala237=
ENST00000688812.1:c.1809A>T	ENSP00000510658.1:p.Ala603=
ENST00000690544.1:c.*1104A>T	ENSP00000508989.1:n.*1104A>T
ENST00000358913.10:c.1833A>T MANE Select	ENSP00000351790.5:p.Ala611=
ENST00000354393.6:c.1008A>T	ENSP00000346369.2:p.Ala336=
ENST00000358913.9:c.1833A>T	ENSP00000351790.5:p.Ala611=
ENST00000540630.5:c.1833A>T	ENSP00000441668.2:p.Ala611=
ENST00000613327.4:c.951A>T	ENSP00000480757.1:p.Ala317=
NM_001256267.1:c.1833A>T	NP_001243196.1:p.Ala611=
NM_001256268.1:c.951A>T	NP_001243197.1:p.Ala317=
NM_032578.3:c.1833A>T , LRG_410t1:c.1833A>T	NP_115967.2:p.Ala611=
NR_045662.3:n.1260A>T
NR_045663.3:n.2101A>T
XM_006718043.2:c.1887A>T	XP_006718106.1:p.Ala629=
XM_011540292.1:c.1863A>T	XP_011538594.1:p.Ala621=
XM_017016833.1:c.1911A>T	XP_016872322.1:p.Ala637=
XM_017016834.2:c.1833A>T	XP_016872323.1:p.Ala611=
XM_024448236.1:c.711A>T	XP_024304004.1:p.Ala237=
NR_045662.4:n.1370A>T
NR_045663.4:n.2046A>T
NM_001256267.2:c.1833A>T	NP_001243196.1:p.Ala611=
NM_001256268.2:c.951A>T	NP_001243197.1:p.Ala317=
NM_032578.4:c.1833A>T MANE Select	NP_115967.2:p.Ala611=