Canonical Allele Identifier: CA376838489

Gene: MYPN

Linked Data

• ClinVar Variation Id: 1519228
• ClinVar RCV Id: RCV002024453 ; RCV002398120
• dbSNP Id: rs1158070956
• MyVariant Identifiers: chr10:g.69925561A>C (hg19) ; chr10:g.68165804A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165804A>C , CM000672.2:g.68165804A>C	GRCh38
NC_000010.10:g.69925561A>C , CM000672.1:g.69925561A>C	GRCh37
NC_000010.9:g.69595567A>C	NCBI36
NG_032118.1:g.64688A>C , LRG_410:g.64688A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.761A>C	ENSP00000346369.2:p.Gln254Pro
ENST00000373675.4:c.1586A>C	ENSP00000362779.4:p.Gln529Pro
ENST00000540630.6:c.1640A>C	ENSP00000441668.3:p.Gln547Pro
ENST00000613327.5:c.1586A>C	ENSP00000480757.2:p.Gln529Pro
ENST00000687572.1:c.464A>C	ENSP00000510427.1:p.Gln155Pro
ENST00000687705.1:c.*1835A>C	ENSP00000509639.1:n.*1835A>C
ENST00000688812.1:c.1562A>C	ENSP00000510658.1:p.Gln521Pro
ENST00000689002.1:n.638A>C
ENST00000690544.1:c.*857A>C	ENSP00000508989.1:n.*857A>C
ENST00000358913.10:c.1586A>C MANE Select	ENSP00000351790.5:p.Gln529Pro
ENST00000354393.6:c.761A>C	ENSP00000346369.2:p.Gln254Pro
ENST00000358913.9:c.1586A>C	ENSP00000351790.5:p.Gln529Pro
ENST00000540630.5:c.1586A>C	ENSP00000441668.2:p.Gln529Pro
ENST00000613327.4:c.704A>C	ENSP00000480757.1:p.Gln235Pro
NM_001256267.1:c.1586A>C	NP_001243196.1:p.Gln529Pro
NM_001256268.1:c.704A>C	NP_001243197.1:p.Gln235Pro
NM_032578.3:c.1586A>C , LRG_410t1:c.1586A>C	NP_115967.2:p.Gln529Pro
NR_045662.3:n.1013A>C
NR_045663.3:n.1854A>C
XM_006718043.2:c.1640A>C	XP_006718106.1:p.Gln547Pro
XM_011540292.1:c.1616A>C	XP_011538594.1:p.Gln539Pro
XM_017016833.1:c.1664A>C	XP_016872322.1:p.Gln555Pro
XM_017016834.2:c.1586A>C	XP_016872323.1:p.Gln529Pro
XM_024448236.1:c.464A>C	XP_024304004.1:p.Gln155Pro
NR_045662.4:n.1123A>C
NR_045663.4:n.1799A>C
NM_001256267.2:c.1586A>C	NP_001243196.1:p.Gln529Pro
NM_001256268.2:c.704A>C	NP_001243197.1:p.Gln235Pro
NM_032578.4:c.1586A>C MANE Select	NP_115967.2:p.Gln529Pro