Canonical Allele Identifier: CA1917232536

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210624G= , CM000672.2:g.68210624G=	GRCh38
NC_000010.10:g.69970381G= , CM000672.1:g.69970381G=	GRCh37
NC_000010.9:g.69640387G=	NCBI36
NG_032118.1:g.109508G= , LRG_410:g.109508G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.*169G=	ENSP00000346369.2:n.*169G=
ENST00000540630.6:c.*169G=	ENSP00000441668.3:n.*169G=
ENST00000613327.5:c.*169G=	ENSP00000480757.2:n.*169G=
ENST00000688812.1:c.*1395G=	ENSP00000510658.1:n.*1395G=
ENST00000690544.1:c.*3403G=	ENSP00000508989.1:n.*3403G=
ENST00000358913.10:c.*169G= MANE Select	ENSP00000351790.5:n.*169G=
ENST00000354393.6:c.*169G=	ENSP00000346369.2:n.*169G=
ENST00000358913.9:c.*169G=	ENSP00000351790.5:n.*169G=
ENST00000540630.5:c.*169G=	ENSP00000441668.2:n.*169G=
ENST00000613327.4:c.*169G=	ENSP00000480757.1:n.*169G=
NM_001256267.1:c.*169G=	NP_001243196.1:n.*169G=
NM_001256268.1:c.*169G=	NP_001243197.1:n.*169G=
NM_032578.3:c.*169G= , LRG_410t1:c.*169G=	NP_115967.2:n.*169G=
NR_045662.3:n.3559G=
NR_045663.3:n.4261G=
XM_006718043.2:c.*169G=	XP_006718106.1:n.*169G=
XM_011540292.1:c.*169G=	XP_011538594.1:n.*169G=
XR_946029.1:n.1574+4664C=
XM_017016833.1:c.*169G=	XP_016872322.1:n.*169G=
XM_017016834.2:c.*169G=	XP_016872323.1:n.*169G=
XM_024448236.1:c.*169G=	XP_024304004.1:n.*169G=
NR_045662.4:n.3669G=
NR_045663.4:n.4206G=
NM_001256267.2:c.*169G=	NP_001243196.1:n.*169G=
NM_001256268.2:c.*169G=	NP_001243197.1:n.*169G=
NM_032578.4:c.*169G= MANE Select	NP_115967.2:n.*169G=