Canonical Allele Identifier: CA1917225575

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195496T= , CM000672.2:g.68195496T=	GRCh38
NC_000010.10:g.69955253T= , CM000672.1:g.69955253T=	GRCh37
NC_000010.9:g.69625259T=	NCBI36
NG_032118.1:g.94380T= , LRG_410:g.94380T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2297T=	ENSP00000346369.2:p.Ile766=
ENST00000540630.6:c.3176T=	ENSP00000441668.3:p.Ile1059=
ENST00000613327.5:c.3122T=	ENSP00000480757.2:p.Ile1041=
ENST00000688812.1:c.*385T=	ENSP00000510658.1:n.*385T=
ENST00000690544.1:c.*2393T=	ENSP00000508989.1:n.*2393T=
ENST00000358913.10:c.3122T= MANE Select	ENSP00000351790.5:p.Ile1041=
ENST00000354393.6:c.2297T=	ENSP00000346369.2:p.Ile766=
ENST00000358913.9:c.3122T=	ENSP00000351790.5:p.Ile1041=
ENST00000540630.5:c.3122T=	ENSP00000441668.2:p.Ile1041=
ENST00000613327.4:c.2240T=	ENSP00000480757.1:p.Ile747=
NM_001256267.1:c.3122T=	NP_001243196.1:p.Ile1041=
NM_001256268.1:c.2240T=	NP_001243197.1:p.Ile747=
NM_032578.3:c.3122T= , LRG_410t1:c.3122T=	NP_115967.2:p.Ile1041=
NR_045662.3:n.2549T=
NR_045663.3:n.3251T=
XM_006718043.2:c.3176T=	XP_006718106.1:p.Ile1059=
XM_011540292.1:c.3152T=	XP_011538594.1:p.Ile1051=
XM_017016833.1:c.3200T=	XP_016872322.1:p.Ile1067=
XM_017016834.2:c.3122T=	XP_016872323.1:p.Ile1041=
XM_024448236.1:c.2000T=	XP_024304004.1:p.Ile667=
NR_045662.4:n.2659T=
NR_045663.4:n.3196T=
NM_001256267.2:c.3122T=	NP_001243196.1:p.Ile1041=
NM_001256268.2:c.2240T=	NP_001243197.1:p.Ile747=
NM_032578.4:c.3122T= MANE Select	NP_115967.2:p.Ile1041=