Canonical Allele Identifier: CA5522947

Gene: MYPN

Linked Data

• dbSNP Id: rs771671403
• ExAC: 10:69955216 A / G
• gnomAD v2: 10-69955216-A-G
• COSMIC: COSM1216501
• MyVariant Identifiers: chr10:g.69955216A>G (hg19) ; chr10:g.68195459A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195459A>G , CM000672.2:g.68195459A>G	GRCh38
NC_000010.10:g.69955216A>G , CM000672.1:g.69955216A>G	GRCh37
NC_000010.9:g.69625222A>G	NCBI36
NG_032118.1:g.94343A>G , LRG_410:g.94343A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000354393.7:c.2260A>G	ENSP00000346369.2:p.Ser754Gly
ENST00000540630.6:c.3139A>G	ENSP00000441668.3:p.Ser1047Gly
ENST00000613327.5:c.3085A>G	ENSP00000480757.2:p.Ser1029Gly
ENST00000688812.1:c.*348A>G	ENSP00000510658.1:n.*348A>G
ENST00000690544.1:c.*2356A>G	ENSP00000508989.1:n.*2356A>G
ENST00000358913.10:c.3085A>G MANE Select	ENSP00000351790.5:p.Ser1029Gly
ENST00000354393.6:c.2260A>G	ENSP00000346369.2:p.Ser754Gly
ENST00000358913.9:c.3085A>G	ENSP00000351790.5:p.Ser1029Gly
ENST00000540630.5:c.3085A>G	ENSP00000441668.2:p.Ser1029Gly
ENST00000613327.4:c.2203A>G	ENSP00000480757.1:p.Ser735Gly
NM_001256267.1:c.3085A>G	NP_001243196.1:p.Ser1029Gly
NM_001256268.1:c.2203A>G	NP_001243197.1:p.Ser735Gly
NM_032578.3:c.3085A>G , LRG_410t1:c.3085A>G	NP_115967.2:p.Ser1029Gly
NR_045662.3:n.2512A>G
NR_045663.3:n.3214A>G
XM_006718043.2:c.3139A>G	XP_006718106.1:p.Ser1047Gly
XM_011540292.1:c.3115A>G	XP_011538594.1:p.Ser1039Gly
XM_017016833.1:c.3163A>G	XP_016872322.1:p.Ser1055Gly
XM_017016834.2:c.3085A>G	XP_016872323.1:p.Ser1029Gly
XM_024448236.1:c.1963A>G	XP_024304004.1:p.Ser655Gly
NR_045662.4:n.2622A>G
NR_045663.4:n.3159A>G
NM_001256267.2:c.3085A>G	NP_001243196.1:p.Ser1029Gly
NM_001256268.2:c.2203A>G	NP_001243197.1:p.Ser735Gly
NM_032578.4:c.3085A>G MANE Select	NP_115967.2:p.Ser1029Gly