Canonical Allele Identifier: CA376839635

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926117T>C (hg19) ; chr10:g.68166360T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166360T>C , CM000672.2:g.68166360T>C	GRCh38
NC_000010.10:g.69926117T>C , CM000672.1:g.69926117T>C	GRCh37
NC_000010.9:g.69596123T>C	NCBI36
NG_032118.1:g.65244T>C , LRG_410:g.65244T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.842T>C	ENSP00000346369.2:p.Ile281Thr
ENST00000373675.4:c.1667T>C	ENSP00000362779.4:p.Ile556Thr
ENST00000540630.6:c.1721T>C	ENSP00000441668.3:p.Ile574Thr
ENST00000613327.5:c.1667T>C	ENSP00000480757.2:p.Ile556Thr
ENST00000687572.1:c.545T>C	ENSP00000510427.1:p.Ile182Thr
ENST00000687705.1:c.*1916T>C	ENSP00000509639.1:n.*1916T>C
ENST00000688812.1:c.1643T>C	ENSP00000510658.1:p.Ile548Thr
ENST00000689002.1:n.719T>C
ENST00000690544.1:c.*938T>C	ENSP00000508989.1:n.*938T>C
ENST00000358913.10:c.1667T>C MANE Select	ENSP00000351790.5:p.Ile556Thr
ENST00000354393.6:c.842T>C	ENSP00000346369.2:p.Ile281Thr
ENST00000358913.9:c.1667T>C	ENSP00000351790.5:p.Ile556Thr
ENST00000540630.5:c.1667T>C	ENSP00000441668.2:p.Ile556Thr
ENST00000613327.4:c.785T>C	ENSP00000480757.1:p.Ile262Thr
NM_001256267.1:c.1667T>C	NP_001243196.1:p.Ile556Thr
NM_001256268.1:c.785T>C	NP_001243197.1:p.Ile262Thr
NM_032578.3:c.1667T>C , LRG_410t1:c.1667T>C	NP_115967.2:p.Ile556Thr
NR_045662.3:n.1094T>C
NR_045663.3:n.1935T>C
XM_006718043.2:c.1721T>C	XP_006718106.1:p.Ile574Thr
XM_011540292.1:c.1697T>C	XP_011538594.1:p.Ile566Thr
XM_017016833.1:c.1745T>C	XP_016872322.1:p.Ile582Thr
XM_017016834.2:c.1667T>C	XP_016872323.1:p.Ile556Thr
XM_024448236.1:c.545T>C	XP_024304004.1:p.Ile182Thr
NR_045662.4:n.1204T>C
NR_045663.4:n.1880T>C
NM_001256267.2:c.1667T>C	NP_001243196.1:p.Ile556Thr
NM_001256268.2:c.785T>C	NP_001243197.1:p.Ile262Thr
NM_032578.4:c.1667T>C MANE Select	NP_115967.2:p.Ile556Thr