Canonical Allele Identifier: CA376847169

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68174499A>C , CM000672.2:g.68174499A>C	GRCh38
NC_000010.10:g.69934256A>C , CM000672.1:g.69934256A>C	GRCh37
NC_000010.9:g.69604262A>C	NCBI36
NG_032118.1:g.73383A>C , LRG_410:g.73383A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.2407A>C MANE Select	NP_115967.2:p.Ser803Arg
ENST00000358913.10:c.2407A>C MANE Select	ENSP00000351790.5:p.Ser803Arg
NM_001256267.1:c.2407A>C	NP_001243196.1:p.Ser803Arg
NM_001256267.2:c.2407A>C	NP_001243196.1:p.Ser803Arg
NM_001256268.1:c.1525A>C	NP_001243197.1:p.Ser509Arg
NM_001256268.2:c.1525A>C	NP_001243197.1:p.Ser509Arg
NM_032578.3:c.2407A>C , LRG_410t1:c.2407A>C	NP_115967.2:p.Ser803Arg
NR_045662.3:n.1834A>C
NR_045662.4:n.1944A>C
NR_045663.3:n.2675A>C
NR_045663.4:n.2620A>C
ENST00000354393.6:c.1582A>C	ENSP00000346369.2:p.Ser528Arg
ENST00000354393.7:c.1582A>C	ENSP00000346369.2:p.Ser528Arg
ENST00000358913.9:c.2407A>C	ENSP00000351790.5:p.Ser803Arg
ENST00000540630.5:c.2407A>C	ENSP00000441668.2:p.Ser803Arg
ENST00000540630.6:c.2461A>C	ENSP00000441668.3:p.Ser821Arg
ENST00000613327.4:c.1525A>C	ENSP00000480757.1:p.Ser509Arg
ENST00000613327.5:c.2407A>C	ENSP00000480757.2:p.Ser803Arg
ENST00000688812.1:c.2383A>C	ENSP00000510658.1:p.Ser795Arg
ENST00000690544.1:c.*1678A>C	ENSP00000508989.1:n.*1678A>C
XM_006718043.2:c.2461A>C	XP_006718106.1:p.Ser821Arg
XM_011540292.1:c.2437A>C	XP_011538594.1:p.Ser813Arg
XM_017016833.1:c.2485A>C	XP_016872322.1:p.Ser829Arg
XM_017016834.2:c.2407A>C	XP_016872323.1:p.Ser803Arg
XM_024448236.1:c.1285A>C	XP_024304004.1:p.Ser429Arg