Canonical Allele Identifier: CA1917227419

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199492C= , CM000672.2:g.68199492C=	GRCh38
NC_000010.10:g.69959249C= , CM000672.1:g.69959249C=	GRCh37
NC_000010.9:g.69629255C=	NCBI36
NG_032118.1:g.98376C= , LRG_410:g.98376C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2585C=	ENSP00000346369.2:p.Thr862=
ENST00000540630.6:c.3464C=	ENSP00000441668.3:p.Thr1155=
ENST00000613327.5:c.3410C=	ENSP00000480757.2:p.Thr1137=
ENST00000688812.1:c.*673C=	ENSP00000510658.1:n.*673C=
ENST00000690544.1:c.*2681C=	ENSP00000508989.1:n.*2681C=
ENST00000358913.10:c.3410C= MANE Select	ENSP00000351790.5:p.Thr1137=
ENST00000354393.6:c.2585C=	ENSP00000346369.2:p.Thr862=
ENST00000358913.9:c.3410C=	ENSP00000351790.5:p.Thr1137=
ENST00000540630.5:c.3410C=	ENSP00000441668.2:p.Thr1137=
ENST00000613327.4:c.2528C=	ENSP00000480757.1:p.Thr843=
NM_001256267.1:c.3410C=	NP_001243196.1:p.Thr1137=
NM_001256268.1:c.2528C=	NP_001243197.1:p.Thr843=
NM_032578.3:c.3410C= , LRG_410t1:c.3410C=	NP_115967.2:p.Thr1137=
NR_045662.3:n.2837C=
NR_045663.3:n.3539C=
XM_006718043.2:c.3464C=	XP_006718106.1:p.Thr1155=
XM_011540292.1:c.3440C=	XP_011538594.1:p.Thr1147=
XR_946029.1:n.1804-217G=
XM_017016833.1:c.3488C=	XP_016872322.1:p.Thr1163=
XM_017016834.2:c.3410C=	XP_016872323.1:p.Thr1137=
XM_024448236.1:c.2288C=	XP_024304004.1:p.Thr763=
NR_045662.4:n.2947C=
NR_045663.4:n.3484C=
NM_001256267.2:c.3410C=	NP_001243196.1:p.Thr1137=
NM_001256268.2:c.2528C=	NP_001243197.1:p.Thr843=
NM_032578.4:c.3410C= MANE Select	NP_115967.2:p.Thr1137=