Canonical Allele Identifier: CA376857248

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69955211G>C (hg19) ; chr10:g.68195454G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195454G>C , CM000672.2:g.68195454G>C	GRCh38
NC_000010.10:g.69955211G>C , CM000672.1:g.69955211G>C	GRCh37
NC_000010.9:g.69625217G>C	NCBI36
NG_032118.1:g.94338G>C , LRG_410:g.94338G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000354393.7:c.2255G>C	ENSP00000346369.2:p.Arg752Thr
ENST00000540630.6:c.3134G>C	ENSP00000441668.3:p.Arg1045Thr
ENST00000613327.5:c.3080G>C	ENSP00000480757.2:p.Arg1027Thr
ENST00000688812.1:c.*343G>C	ENSP00000510658.1:n.*343G>C
ENST00000690544.1:c.*2351G>C	ENSP00000508989.1:n.*2351G>C
ENST00000358913.10:c.3080G>C MANE Select	ENSP00000351790.5:p.Arg1027Thr
ENST00000354393.6:c.2255G>C	ENSP00000346369.2:p.Arg752Thr
ENST00000358913.9:c.3080G>C	ENSP00000351790.5:p.Arg1027Thr
ENST00000540630.5:c.3080G>C	ENSP00000441668.2:p.Arg1027Thr
ENST00000613327.4:c.2198G>C	ENSP00000480757.1:p.Arg733Thr
NM_001256267.1:c.3080G>C	NP_001243196.1:p.Arg1027Thr
NM_001256268.1:c.2198G>C	NP_001243197.1:p.Arg733Thr
NM_032578.3:c.3080G>C , LRG_410t1:c.3080G>C	NP_115967.2:p.Arg1027Thr
NR_045662.3:n.2507G>C
NR_045663.3:n.3209G>C
XM_006718043.2:c.3134G>C	XP_006718106.1:p.Arg1045Thr
XM_011540292.1:c.3110G>C	XP_011538594.1:p.Arg1037Thr
XM_017016833.1:c.3158G>C	XP_016872322.1:p.Arg1053Thr
XM_017016834.2:c.3080G>C	XP_016872323.1:p.Arg1027Thr
XM_024448236.1:c.1958G>C	XP_024304004.1:p.Arg653Thr
NR_045662.4:n.2617G>C
NR_045663.4:n.3154G>C
NM_001256267.2:c.3080G>C	NP_001243196.1:p.Arg1027Thr
NM_001256268.2:c.2198G>C	NP_001243197.1:p.Arg733Thr
NM_032578.4:c.3080G>C MANE Select	NP_115967.2:p.Arg1027Thr