Canonical Allele Identifier: CA469805192

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69925572A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165815A>C , CM000672.2:g.68165815A>C	GRCh38
NC_000010.10:g.69925572A>C , CM000672.1:g.69925572A>C	GRCh37
NC_000010.9:g.69595578A>C	NCBI36
NG_032118.1:g.64699A>C , LRG_410:g.64699A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.772A>C	ENSP00000346369.2:p.Arg258=
ENST00000373675.4:c.1597A>C	ENSP00000362779.4:p.Arg533=
ENST00000540630.6:c.1651A>C	ENSP00000441668.3:p.Arg551=
ENST00000613327.5:c.1597A>C	ENSP00000480757.2:p.Arg533=
ENST00000687572.1:c.475A>C	ENSP00000510427.1:p.Arg159=
ENST00000687705.1:c.*1846A>C	ENSP00000509639.1:n.*1846A>C
ENST00000688812.1:c.1573A>C	ENSP00000510658.1:p.Arg525=
ENST00000689002.1:n.649A>C
ENST00000690544.1:c.*868A>C	ENSP00000508989.1:n.*868A>C
ENST00000358913.10:c.1597A>C MANE Select	ENSP00000351790.5:p.Arg533=
ENST00000354393.6:c.772A>C	ENSP00000346369.2:p.Arg258=
ENST00000358913.9:c.1597A>C	ENSP00000351790.5:p.Arg533=
ENST00000540630.5:c.1597A>C	ENSP00000441668.2:p.Arg533=
ENST00000613327.4:c.715A>C	ENSP00000480757.1:p.Arg239=
NM_001256267.1:c.1597A>C	NP_001243196.1:p.Arg533=
NM_001256268.1:c.715A>C	NP_001243197.1:p.Arg239=
NM_032578.3:c.1597A>C , LRG_410t1:c.1597A>C	NP_115967.2:p.Arg533=
NR_045662.3:n.1024A>C
NR_045663.3:n.1865A>C
XM_006718043.2:c.1651A>C	XP_006718106.1:p.Arg551=
XM_011540292.1:c.1627A>C	XP_011538594.1:p.Arg543=
XM_017016833.1:c.1675A>C	XP_016872322.1:p.Arg559=
XM_017016834.2:c.1597A>C	XP_016872323.1:p.Arg533=
XM_024448236.1:c.475A>C	XP_024304004.1:p.Arg159=
NR_045662.4:n.1134A>C
NR_045663.4:n.1810A>C
NM_001256267.2:c.1597A>C	NP_001243196.1:p.Arg533=
NM_001256268.2:c.715A>C	NP_001243197.1:p.Arg239=
NM_032578.4:c.1597A>C MANE Select	NP_115967.2:p.Arg533=