Canonical Allele Identifier: CA1917227337

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199317T= , CM000672.2:g.68199317T=	GRCh38
NC_000010.10:g.69959074T= , CM000672.1:g.69959074T=	GRCh37
NC_000010.9:g.69629080T=	NCBI36
NG_032118.1:g.98201T= , LRG_410:g.98201T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2461-51T=	ENSP00000346369.2:n.2461-51T=
ENST00000540630.6:c.3340-51T=	ENSP00000441668.3:n.3340-51T=
ENST00000613327.5:c.3286-51T=	ENSP00000480757.2:n.3286-51T=
ENST00000688812.1:c.*549-51T=	ENSP00000510658.1:n.*549-51T=
ENST00000690544.1:c.*2557-51T=	ENSP00000508989.1:n.*2557-51T=
ENST00000358913.10:c.3286-51T= MANE Select	ENSP00000351790.5:n.3286-51T=
ENST00000354393.6:c.2461-51T=	ENSP00000346369.2:n.2461-51T=
ENST00000358913.9:c.3286-51T=	ENSP00000351790.5:n.3286-51T=
ENST00000540630.5:c.3286-51T=	ENSP00000441668.2:n.3286-51T=
ENST00000613327.4:c.2404-51T=	ENSP00000480757.1:n.2404-51T=
NM_001256267.1:c.3286-51T=	NP_001243196.1:n.3286-51T=
NM_001256268.1:c.2404-51T=	NP_001243197.1:n.2404-51T=
NM_032578.3:c.3286-51T= , LRG_410t1:c.3286-51T=	NP_115967.2:n.3286-51T=
NR_045662.3:n.2713-51T=
NR_045663.3:n.3415-51T=
XM_006718043.2:c.3340-51T=	XP_006718106.1:n.3340-51T=
XM_011540292.1:c.3316-51T=	XP_011538594.1:n.3316-51T=
XR_946029.1:n.1804-42A=
XM_017016833.1:c.3364-51T=	XP_016872322.1:n.3364-51T=
XM_017016834.2:c.3286-51T=	XP_016872323.1:n.3286-51T=
XM_024448236.1:c.2164-51T=	XP_024304004.1:n.2164-51T=
NR_045662.4:n.2823-51T=
NR_045663.4:n.3360-51T=
NM_001256267.2:c.3286-51T=	NP_001243196.1:n.3286-51T=
NM_001256268.2:c.2404-51T=	NP_001243197.1:n.2404-51T=
NM_032578.4:c.3286-51T= MANE Select	NP_115967.2:n.3286-51T=