Canonical Allele Identifier: CA1917225569

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195481T= , CM000672.2:g.68195481T=	GRCh38
NC_000010.10:g.69955238T= , CM000672.1:g.69955238T=	GRCh37
NC_000010.9:g.69625244T=	NCBI36
NG_032118.1:g.94365T= , LRG_410:g.94365T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2282T=	ENSP00000346369.2:p.Val761=
ENST00000540630.6:c.3161T=	ENSP00000441668.3:p.Val1054=
ENST00000613327.5:c.3107T=	ENSP00000480757.2:p.Val1036=
ENST00000688812.1:c.*370T=	ENSP00000510658.1:n.*370T=
ENST00000690544.1:c.*2378T=	ENSP00000508989.1:n.*2378T=
ENST00000358913.10:c.3107T= MANE Select	ENSP00000351790.5:p.Val1036=
ENST00000354393.6:c.2282T=	ENSP00000346369.2:p.Val761=
ENST00000358913.9:c.3107T=	ENSP00000351790.5:p.Val1036=
ENST00000540630.5:c.3107T=	ENSP00000441668.2:p.Val1036=
ENST00000613327.4:c.2225T=	ENSP00000480757.1:p.Val742=
NM_001256267.1:c.3107T=	NP_001243196.1:p.Val1036=
NM_001256268.1:c.2225T=	NP_001243197.1:p.Val742=
NM_032578.3:c.3107T= , LRG_410t1:c.3107T=	NP_115967.2:p.Val1036=
NR_045662.3:n.2534T=
NR_045663.3:n.3236T=
XM_006718043.2:c.3161T=	XP_006718106.1:p.Val1054=
XM_011540292.1:c.3137T=	XP_011538594.1:p.Val1046=
XM_017016833.1:c.3185T=	XP_016872322.1:p.Val1062=
XM_017016834.2:c.3107T=	XP_016872323.1:p.Val1036=
XM_024448236.1:c.1985T=	XP_024304004.1:p.Val662=
NR_045662.4:n.2644T=
NR_045663.4:n.3181T=
NM_001256267.2:c.3107T=	NP_001243196.1:p.Val1036=
NM_001256268.2:c.2225T=	NP_001243197.1:p.Val742=
NM_032578.4:c.3107T= MANE Select	NP_115967.2:p.Val1036=