Canonical Allele Identifier: CA376857281

Gene: MYPN

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000354393.7:c.2258T>G	ENSP00000346369.2:p.Ile753Ser
ENST00000540630.6:c.3137T>G	ENSP00000441668.3:p.Ile1046Ser
ENST00000613327.5:c.3083T>G	ENSP00000480757.2:p.Ile1028Ser
ENST00000688812.1:c.*346T>G	ENSP00000510658.1:n.*346T>G
ENST00000690544.1:c.*2354T>G	ENSP00000508989.1:n.*2354T>G
ENST00000358913.10:c.3083T>G MANE Select	ENSP00000351790.5:p.Ile1028Ser
ENST00000354393.6:c.2258T>G	ENSP00000346369.2:p.Ile753Ser
ENST00000358913.9:c.3083T>G	ENSP00000351790.5:p.Ile1028Ser
ENST00000540630.5:c.3083T>G	ENSP00000441668.2:p.Ile1028Ser
ENST00000613327.4:c.2201T>G	ENSP00000480757.1:p.Ile734Ser
NM_001256267.1:c.3083T>G	NP_001243196.1:p.Ile1028Ser
NM_001256268.1:c.2201T>G	NP_001243197.1:p.Ile734Ser
NM_032578.3:c.3083T>G , LRG_410t1:c.3083T>G	NP_115967.2:p.Ile1028Ser
NR_045662.3:n.2510T>G
NR_045663.3:n.3212T>G
XM_006718043.2:c.3137T>G	XP_006718106.1:p.Ile1046Ser
XM_011540292.1:c.3113T>G	XP_011538594.1:p.Ile1038Ser
XM_017016833.1:c.3161T>G	XP_016872322.1:p.Ile1054Ser
XM_017016834.2:c.3083T>G	XP_016872323.1:p.Ile1028Ser
XM_024448236.1:c.1961T>G	XP_024304004.1:p.Ile654Ser
NR_045662.4:n.2620T>G
NR_045663.4:n.3157T>G
NM_001256267.2:c.3083T>G	NP_001243196.1:p.Ile1028Ser
NM_001256268.2:c.2201T>G	NP_001243197.1:p.Ile734Ser
NM_032578.4:c.3083T>G MANE Select	NP_115967.2:p.Ile1028Ser