Canonical Allele Identifier: CA376857283

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69955215C>G (hg19) ; chr10:g.68195458C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195458C>G , CM000672.2:g.68195458C>G	GRCh38
NC_000010.10:g.69955215C>G , CM000672.1:g.69955215C>G	GRCh37
NC_000010.9:g.69625221C>G	NCBI36
NG_032118.1:g.94342C>G , LRG_410:g.94342C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000354393.7:c.2259C>G	ENSP00000346369.2:p.Ile753Met
ENST00000540630.6:c.3138C>G	ENSP00000441668.3:p.Ile1046Met
ENST00000613327.5:c.3084C>G	ENSP00000480757.2:p.Ile1028Met
ENST00000688812.1:c.*347C>G	ENSP00000510658.1:n.*347C>G
ENST00000690544.1:c.*2355C>G	ENSP00000508989.1:n.*2355C>G
ENST00000358913.10:c.3084C>G MANE Select	ENSP00000351790.5:p.Ile1028Met
ENST00000354393.6:c.2259C>G	ENSP00000346369.2:p.Ile753Met
ENST00000358913.9:c.3084C>G	ENSP00000351790.5:p.Ile1028Met
ENST00000540630.5:c.3084C>G	ENSP00000441668.2:p.Ile1028Met
ENST00000613327.4:c.2202C>G	ENSP00000480757.1:p.Ile734Met
NM_001256267.1:c.3084C>G	NP_001243196.1:p.Ile1028Met
NM_001256268.1:c.2202C>G	NP_001243197.1:p.Ile734Met
NM_032578.3:c.3084C>G , LRG_410t1:c.3084C>G	NP_115967.2:p.Ile1028Met
NR_045662.3:n.2511C>G
NR_045663.3:n.3213C>G
XM_006718043.2:c.3138C>G	XP_006718106.1:p.Ile1046Met
XM_011540292.1:c.3114C>G	XP_011538594.1:p.Ile1038Met
XM_017016833.1:c.3162C>G	XP_016872322.1:p.Ile1054Met
XM_017016834.2:c.3084C>G	XP_016872323.1:p.Ile1028Met
XM_024448236.1:c.1962C>G	XP_024304004.1:p.Ile654Met
NR_045662.4:n.2621C>G
NR_045663.4:n.3158C>G
NM_001256267.2:c.3084C>G	NP_001243196.1:p.Ile1028Met
NM_001256268.2:c.2202C>G	NP_001243197.1:p.Ile734Met
NM_032578.4:c.3084C>G MANE Select	NP_115967.2:p.Ile1028Met