Canonical Allele Identifier: CA376859319

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199518T>C , CM000672.2:g.68199518T>C	GRCh38
NC_000010.10:g.69959275T>C , CM000672.1:g.69959275T>C	GRCh37
NC_000010.9:g.69629281T>C	NCBI36
NG_032118.1:g.98402T>C , LRG_410:g.98402T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3436T>C MANE Select	NP_115967.2:p.Cys1146Arg
ENST00000358913.10:c.3436T>C MANE Select	ENSP00000351790.5:p.Cys1146Arg
NM_001256267.1:c.3436T>C	NP_001243196.1:p.Cys1146Arg
NM_001256267.2:c.3436T>C	NP_001243196.1:p.Cys1146Arg
NM_001256268.1:c.2554T>C	NP_001243197.1:p.Cys852Arg
NM_001256268.2:c.2554T>C	NP_001243197.1:p.Cys852Arg
NM_032578.3:c.3436T>C , LRG_410t1:c.3436T>C	NP_115967.2:p.Cys1146Arg
NR_045662.3:n.2863T>C
NR_045662.4:n.2973T>C
NR_045663.3:n.3565T>C
NR_045663.4:n.3510T>C
ENST00000354393.6:c.2611T>C	ENSP00000346369.2:p.Cys871Arg
ENST00000354393.7:c.2611T>C	ENSP00000346369.2:p.Cys871Arg
ENST00000358913.9:c.3436T>C	ENSP00000351790.5:p.Cys1146Arg
ENST00000540630.5:c.3436T>C	ENSP00000441668.2:p.Cys1146Arg
ENST00000540630.6:c.3490T>C	ENSP00000441668.3:p.Cys1164Arg
ENST00000613327.4:c.2554T>C	ENSP00000480757.1:p.Cys852Arg
ENST00000613327.5:c.3436T>C	ENSP00000480757.2:p.Cys1146Arg
ENST00000688812.1:c.*699T>C	ENSP00000510658.1:n.*699T>C
ENST00000690544.1:c.*2707T>C	ENSP00000508989.1:n.*2707T>C
XM_006718043.2:c.3490T>C	XP_006718106.1:p.Cys1164Arg
XM_011540292.1:c.3466T>C	XP_011538594.1:p.Cys1156Arg
XM_017016833.1:c.3514T>C	XP_016872322.1:p.Cys1172Arg
XM_017016834.2:c.3436T>C	XP_016872323.1:p.Cys1146Arg
XM_024448236.1:c.2314T>C	XP_024304004.1:p.Cys772Arg
XR_946029.1:n.1804-243A>G