Canonical Allele Identifier: CA1917225568

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195479G= , CM000672.2:g.68195479G=	GRCh38
NC_000010.10:g.69955236G= , CM000672.1:g.69955236G=	GRCh37
NC_000010.9:g.69625242G=	NCBI36
NG_032118.1:g.94363G= , LRG_410:g.94363G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2280G=	ENSP00000346369.2:p.Met760=
ENST00000540630.6:c.3159G=	ENSP00000441668.3:p.Met1053=
ENST00000613327.5:c.3105G=	ENSP00000480757.2:p.Met1035=
ENST00000688812.1:c.*368G=	ENSP00000510658.1:n.*368G=
ENST00000690544.1:c.*2376G=	ENSP00000508989.1:n.*2376G=
ENST00000358913.10:c.3105G= MANE Select	ENSP00000351790.5:p.Met1035=
ENST00000354393.6:c.2280G=	ENSP00000346369.2:p.Met760=
ENST00000358913.9:c.3105G=	ENSP00000351790.5:p.Met1035=
ENST00000540630.5:c.3105G=	ENSP00000441668.2:p.Met1035=
ENST00000613327.4:c.2223G=	ENSP00000480757.1:p.Met741=
NM_001256267.1:c.3105G=	NP_001243196.1:p.Met1035=
NM_001256268.1:c.2223G=	NP_001243197.1:p.Met741=
NM_032578.3:c.3105G= , LRG_410t1:c.3105G=	NP_115967.2:p.Met1035=
NR_045662.3:n.2532G=
NR_045663.3:n.3234G=
XM_006718043.2:c.3159G=	XP_006718106.1:p.Met1053=
XM_011540292.1:c.3135G=	XP_011538594.1:p.Met1045=
XM_017016833.1:c.3183G=	XP_016872322.1:p.Met1061=
XM_017016834.2:c.3105G=	XP_016872323.1:p.Met1035=
XM_024448236.1:c.1983G=	XP_024304004.1:p.Met661=
NR_045662.4:n.2642G=
NR_045663.4:n.3179G=
NM_001256267.2:c.3105G=	NP_001243196.1:p.Met1035=
NM_001256268.2:c.2223G=	NP_001243197.1:p.Met741=
NM_032578.4:c.3105G= MANE Select	NP_115967.2:p.Met1035=