Canonical Allele Identifier: CA1917226439

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68197369A= , CM000672.2:g.68197369A=	GRCh38
NC_000010.10:g.69957126A= , CM000672.1:g.69957126A=	GRCh37
NC_000010.9:g.69627132A=	NCBI36
NG_032118.1:g.96253A= , LRG_410:g.96253A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2351A=	ENSP00000346369.2:p.Gln784=
ENST00000540630.6:c.3230A=	ENSP00000441668.3:p.Gln1077=
ENST00000613327.5:c.3176A=	ENSP00000480757.2:p.Gln1059=
ENST00000688812.1:c.*439A=	ENSP00000510658.1:n.*439A=
ENST00000690544.1:c.*2447A=	ENSP00000508989.1:n.*2447A=
ENST00000358913.10:c.3176A= MANE Select	ENSP00000351790.5:p.Gln1059=
ENST00000354393.6:c.2351A=	ENSP00000346369.2:p.Gln784=
ENST00000358913.9:c.3176A=	ENSP00000351790.5:p.Gln1059=
ENST00000540630.5:c.3176A=	ENSP00000441668.2:p.Gln1059=
ENST00000613327.4:c.2294A=	ENSP00000480757.1:p.Gln765=
NM_001256267.1:c.3176A=	NP_001243196.1:p.Gln1059=
NM_001256268.1:c.2294A=	NP_001243197.1:p.Gln765=
NM_032578.3:c.3176A= , LRG_410t1:c.3176A=	NP_115967.2:p.Gln1059=
NR_045662.3:n.2603A=
NR_045663.3:n.3305A=
XM_006718043.2:c.3230A=	XP_006718106.1:p.Gln1077=
XM_011540292.1:c.3206A=	XP_011538594.1:p.Gln1069=
XM_017016833.1:c.3254A=	XP_016872322.1:p.Gln1085=
XM_017016834.2:c.3176A=	XP_016872323.1:p.Gln1059=
XM_024448236.1:c.2054A=	XP_024304004.1:p.Gln685=
NR_045662.4:n.2713A=
NR_045663.4:n.3250A=
NM_001256267.2:c.3176A=	NP_001243196.1:p.Gln1059=
NM_001256268.2:c.2294A=	NP_001243197.1:p.Gln765=
NM_032578.4:c.3176A= MANE Select	NP_115967.2:p.Gln1059=