Canonical Allele Identifier: CA376858892

Gene: MYPN

Linked Data

• dbSNP Id: rs2134299299
• MyVariant Identifiers: chr10:g.69959137C>A (hg19) ; chr10:g.68199380C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199380C>A , CM000672.2:g.68199380C>A	GRCh38
NC_000010.10:g.69959137C>A , CM000672.1:g.69959137C>A	GRCh37
NC_000010.9:g.69629143C>A	NCBI36
NG_032118.1:g.98264C>A , LRG_410:g.98264C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2473C>A	ENSP00000346369.2:p.Pro825Thr
ENST00000540630.6:c.3352C>A	ENSP00000441668.3:p.Pro1118Thr
ENST00000613327.5:c.3298C>A	ENSP00000480757.2:p.Pro1100Thr
ENST00000688812.1:c.*561C>A	ENSP00000510658.1:n.*561C>A
ENST00000690544.1:c.*2569C>A	ENSP00000508989.1:n.*2569C>A
ENST00000358913.10:c.3298C>A MANE Select	ENSP00000351790.5:p.Pro1100Thr
ENST00000354393.6:c.2473C>A	ENSP00000346369.2:p.Pro825Thr
ENST00000358913.9:c.3298C>A	ENSP00000351790.5:p.Pro1100Thr
ENST00000540630.5:c.3298C>A	ENSP00000441668.2:p.Pro1100Thr
ENST00000613327.4:c.2416C>A	ENSP00000480757.1:p.Pro806Thr
NM_001256267.1:c.3298C>A	NP_001243196.1:p.Pro1100Thr
NM_001256268.1:c.2416C>A	NP_001243197.1:p.Pro806Thr
NM_032578.3:c.3298C>A , LRG_410t1:c.3298C>A	NP_115967.2:p.Pro1100Thr
NR_045662.3:n.2725C>A
NR_045663.3:n.3427C>A
XM_006718043.2:c.3352C>A	XP_006718106.1:p.Pro1118Thr
XM_011540292.1:c.3328C>A	XP_011538594.1:p.Pro1110Thr
XR_946029.1:n.1804-105G>T
XM_017016833.1:c.3376C>A	XP_016872322.1:p.Pro1126Thr
XM_017016834.2:c.3298C>A	XP_016872323.1:p.Pro1100Thr
XM_024448236.1:c.2176C>A	XP_024304004.1:p.Pro726Thr
NR_045662.4:n.2835C>A
NR_045663.4:n.3372C>A
NM_001256267.2:c.3298C>A	NP_001243196.1:p.Pro1100Thr
NM_001256268.2:c.2416C>A	NP_001243197.1:p.Pro806Thr
NM_032578.4:c.3298C>A MANE Select	NP_115967.2:p.Pro1100Thr