Canonical Allele Identifier: CA376857279

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69955214T>C (hg19) ; chr10:g.68195457T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195457T>C , CM000672.2:g.68195457T>C	GRCh38
NC_000010.10:g.69955214T>C , CM000672.1:g.69955214T>C	GRCh37
NC_000010.9:g.69625220T>C	NCBI36
NG_032118.1:g.94341T>C , LRG_410:g.94341T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000354393.7:c.2258T>C	ENSP00000346369.2:p.Ile753Thr
ENST00000540630.6:c.3137T>C	ENSP00000441668.3:p.Ile1046Thr
ENST00000613327.5:c.3083T>C	ENSP00000480757.2:p.Ile1028Thr
ENST00000688812.1:c.*346T>C	ENSP00000510658.1:n.*346T>C
ENST00000690544.1:c.*2354T>C	ENSP00000508989.1:n.*2354T>C
ENST00000358913.10:c.3083T>C MANE Select	ENSP00000351790.5:p.Ile1028Thr
ENST00000354393.6:c.2258T>C	ENSP00000346369.2:p.Ile753Thr
ENST00000358913.9:c.3083T>C	ENSP00000351790.5:p.Ile1028Thr
ENST00000540630.5:c.3083T>C	ENSP00000441668.2:p.Ile1028Thr
ENST00000613327.4:c.2201T>C	ENSP00000480757.1:p.Ile734Thr
NM_001256267.1:c.3083T>C	NP_001243196.1:p.Ile1028Thr
NM_001256268.1:c.2201T>C	NP_001243197.1:p.Ile734Thr
NM_032578.3:c.3083T>C , LRG_410t1:c.3083T>C	NP_115967.2:p.Ile1028Thr
NR_045662.3:n.2510T>C
NR_045663.3:n.3212T>C
XM_006718043.2:c.3137T>C	XP_006718106.1:p.Ile1046Thr
XM_011540292.1:c.3113T>C	XP_011538594.1:p.Ile1038Thr
XM_017016833.1:c.3161T>C	XP_016872322.1:p.Ile1054Thr
XM_017016834.2:c.3083T>C	XP_016872323.1:p.Ile1028Thr
XM_024448236.1:c.1961T>C	XP_024304004.1:p.Ile654Thr
NR_045662.4:n.2620T>C
NR_045663.4:n.3157T>C
NM_001256267.2:c.3083T>C	NP_001243196.1:p.Ile1028Thr
NM_001256268.2:c.2201T>C	NP_001243197.1:p.Ile734Thr
NM_032578.4:c.3083T>C MANE Select	NP_115967.2:p.Ile1028Thr