Canonical Allele Identifier: CA469812119

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69955210A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195453A>C , CM000672.2:g.68195453A>C	GRCh38
NC_000010.10:g.69955210A>C , CM000672.1:g.69955210A>C	GRCh37
NC_000010.9:g.69625216A>C	NCBI36
NG_032118.1:g.94337A>C , LRG_410:g.94337A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000354393.7:c.2254A>C	ENSP00000346369.2:p.Arg752=
ENST00000540630.6:c.3133A>C	ENSP00000441668.3:p.Arg1045=
ENST00000613327.5:c.3079A>C	ENSP00000480757.2:p.Arg1027=
ENST00000688812.1:c.*342A>C	ENSP00000510658.1:n.*342A>C
ENST00000690544.1:c.*2350A>C	ENSP00000508989.1:n.*2350A>C
ENST00000358913.10:c.3079A>C MANE Select	ENSP00000351790.5:p.Arg1027=
ENST00000354393.6:c.2254A>C	ENSP00000346369.2:p.Arg752=
ENST00000358913.9:c.3079A>C	ENSP00000351790.5:p.Arg1027=
ENST00000540630.5:c.3079A>C	ENSP00000441668.2:p.Arg1027=
ENST00000613327.4:c.2197A>C	ENSP00000480757.1:p.Arg733=
NM_001256267.1:c.3079A>C	NP_001243196.1:p.Arg1027=
NM_001256268.1:c.2197A>C	NP_001243197.1:p.Arg733=
NM_032578.3:c.3079A>C , LRG_410t1:c.3079A>C	NP_115967.2:p.Arg1027=
NR_045662.3:n.2506A>C
NR_045663.3:n.3208A>C
XM_006718043.2:c.3133A>C	XP_006718106.1:p.Arg1045=
XM_011540292.1:c.3109A>C	XP_011538594.1:p.Arg1037=
XM_017016833.1:c.3157A>C	XP_016872322.1:p.Arg1053=
XM_017016834.2:c.3079A>C	XP_016872323.1:p.Arg1027=
XM_024448236.1:c.1957A>C	XP_024304004.1:p.Arg653=
NR_045662.4:n.2616A>C
NR_045663.4:n.3153A>C
NM_001256267.2:c.3079A>C	NP_001243196.1:p.Arg1027=
NM_001256268.2:c.2197A>C	NP_001243197.1:p.Arg733=
NM_032578.4:c.3079A>C MANE Select	NP_115967.2:p.Arg1027=