Canonical Allele Identifier: CA1917225503

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195305A= , CM000672.2:g.68195305A=	GRCh38
NC_000010.10:g.69955062A= , CM000672.1:g.69955062A=	GRCh37
NC_000010.9:g.69625068A=	NCBI36
NG_032118.1:g.94189A= , LRG_410:g.94189A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2251-145A=	ENSP00000346369.2:n.2251-145A=
ENST00000540630.6:c.3130-145A=	ENSP00000441668.3:n.3130-145A=
ENST00000613327.5:c.3076-145A=	ENSP00000480757.2:n.3076-145A=
ENST00000688812.1:c.*339-145A=	ENSP00000510658.1:n.*339-145A=
ENST00000690544.1:c.*2347-145A=	ENSP00000508989.1:n.*2347-145A=
ENST00000358913.10:c.3076-145A= MANE Select	ENSP00000351790.5:n.3076-145A=
ENST00000354393.6:c.2251-145A=	ENSP00000346369.2:n.2251-145A=
ENST00000358913.9:c.3076-145A=	ENSP00000351790.5:n.3076-145A=
ENST00000540630.5:c.3076-145A=	ENSP00000441668.2:n.3076-145A=
ENST00000613327.4:c.2194-145A=	ENSP00000480757.1:n.2194-145A=
NM_001256267.1:c.3076-145A=	NP_001243196.1:n.3076-145A=
NM_001256268.1:c.2194-145A=	NP_001243197.1:n.2194-145A=
NM_032578.3:c.3076-145A= , LRG_410t1:c.3076-145A=	NP_115967.2:n.3076-145A=
NR_045662.3:n.2503-145A=
NR_045663.3:n.3205-145A=
XM_006718043.2:c.3130-145A=	XP_006718106.1:n.3130-145A=
XM_011540292.1:c.3106-145A=	XP_011538594.1:n.3106-145A=
XM_017016833.1:c.3154-145A=	XP_016872322.1:n.3154-145A=
XM_017016834.2:c.3076-145A=	XP_016872323.1:n.3076-145A=
XM_024448236.1:c.1954-145A=	XP_024304004.1:n.1954-145A=
NR_045662.4:n.2613-145A=
NR_045663.4:n.3150-145A=
NM_001256267.2:c.3076-145A=	NP_001243196.1:n.3076-145A=
NM_001256268.2:c.2194-145A=	NP_001243197.1:n.2194-145A=
NM_032578.4:c.3076-145A= MANE Select	NP_115967.2:n.3076-145A=