Canonical Allele Identifier: CA1917225587

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195518T= , CM000672.2:g.68195518T=	GRCh38
NC_000010.10:g.69955275T= , CM000672.1:g.69955275T=	GRCh37
NC_000010.9:g.69625281T=	NCBI36
NG_032118.1:g.94402T= , LRG_410:g.94402T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2319T=	ENSP00000346369.2:p.Ala773=
ENST00000540630.6:c.3198T=	ENSP00000441668.3:p.Ala1066=
ENST00000613327.5:c.3144T=	ENSP00000480757.2:p.Ala1048=
ENST00000688812.1:c.*407T=	ENSP00000510658.1:n.*407T=
ENST00000690544.1:c.*2415T=	ENSP00000508989.1:n.*2415T=
ENST00000358913.10:c.3144T= MANE Select	ENSP00000351790.5:p.Ala1048=
ENST00000354393.6:c.2319T=	ENSP00000346369.2:p.Ala773=
ENST00000358913.9:c.3144T=	ENSP00000351790.5:p.Ala1048=
ENST00000540630.5:c.3144T=	ENSP00000441668.2:p.Ala1048=
ENST00000613327.4:c.2262T=	ENSP00000480757.1:p.Ala754=
NM_001256267.1:c.3144T=	NP_001243196.1:p.Ala1048=
NM_001256268.1:c.2262T=	NP_001243197.1:p.Ala754=
NM_032578.3:c.3144T= , LRG_410t1:c.3144T=	NP_115967.2:p.Ala1048=
NR_045662.3:n.2571T=
NR_045663.3:n.3273T=
XM_006718043.2:c.3198T=	XP_006718106.1:p.Ala1066=
XM_011540292.1:c.3174T=	XP_011538594.1:p.Ala1058=
XM_017016833.1:c.3222T=	XP_016872322.1:p.Ala1074=
XM_017016834.2:c.3144T=	XP_016872323.1:p.Ala1048=
XM_024448236.1:c.2022T=	XP_024304004.1:p.Ala674=
NR_045662.4:n.2681T=
NR_045663.4:n.3218T=
NM_001256267.2:c.3144T=	NP_001243196.1:p.Ala1048=
NM_001256268.2:c.2262T=	NP_001243197.1:p.Ala754=
NM_032578.4:c.3144T= MANE Select	NP_115967.2:p.Ala1048=