Canonical Allele Identifier: CA376838511

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69925567A>C (hg19) ; chr10:g.68165810A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165810A>C , CM000672.2:g.68165810A>C	GRCh38
NC_000010.10:g.69925567A>C , CM000672.1:g.69925567A>C	GRCh37
NC_000010.9:g.69595573A>C	NCBI36
NG_032118.1:g.64694A>C , LRG_410:g.64694A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.767A>C	ENSP00000346369.2:p.His256Pro
ENST00000373675.4:c.1592A>C	ENSP00000362779.4:p.His531Pro
ENST00000540630.6:c.1646A>C	ENSP00000441668.3:p.His549Pro
ENST00000613327.5:c.1592A>C	ENSP00000480757.2:p.His531Pro
ENST00000687572.1:c.470A>C	ENSP00000510427.1:p.His157Pro
ENST00000687705.1:c.*1841A>C	ENSP00000509639.1:n.*1841A>C
ENST00000688812.1:c.1568A>C	ENSP00000510658.1:p.His523Pro
ENST00000689002.1:n.644A>C
ENST00000690544.1:c.*863A>C	ENSP00000508989.1:n.*863A>C
ENST00000358913.10:c.1592A>C MANE Select	ENSP00000351790.5:p.His531Pro
ENST00000354393.6:c.767A>C	ENSP00000346369.2:p.His256Pro
ENST00000358913.9:c.1592A>C	ENSP00000351790.5:p.His531Pro
ENST00000540630.5:c.1592A>C	ENSP00000441668.2:p.His531Pro
ENST00000613327.4:c.710A>C	ENSP00000480757.1:p.His237Pro
NM_001256267.1:c.1592A>C	NP_001243196.1:p.His531Pro
NM_001256268.1:c.710A>C	NP_001243197.1:p.His237Pro
NM_032578.3:c.1592A>C , LRG_410t1:c.1592A>C	NP_115967.2:p.His531Pro
NR_045662.3:n.1019A>C
NR_045663.3:n.1860A>C
XM_006718043.2:c.1646A>C	XP_006718106.1:p.His549Pro
XM_011540292.1:c.1622A>C	XP_011538594.1:p.His541Pro
XM_017016833.1:c.1670A>C	XP_016872322.1:p.His557Pro
XM_017016834.2:c.1592A>C	XP_016872323.1:p.His531Pro
XM_024448236.1:c.470A>C	XP_024304004.1:p.His157Pro
NR_045662.4:n.1129A>C
NR_045663.4:n.1805A>C
NM_001256267.2:c.1592A>C	NP_001243196.1:p.His531Pro
NM_001256268.2:c.710A>C	NP_001243197.1:p.His237Pro
NM_032578.4:c.1592A>C MANE Select	NP_115967.2:p.His531Pro