Canonical Allele Identifier: CA5522601

Gene: MYPN

Linked Data

• dbSNP Id: rs750750351
• ExAC: 10:69925479 A / G
• gnomAD v2: 10-69925479-A-G
• gnomAD v3: 10-68165722-A-G
• gnomAD v4: 10-68165722-A-G
• MyVariant Identifiers: chr10:g.69925479A>G (hg19) ; chr10:g.68165722A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165722A>G , CM000672.2:g.68165722A>G	GRCh38
NC_000010.10:g.69925479A>G , CM000672.1:g.69925479A>G	GRCh37
NC_000010.9:g.69595485A>G	NCBI36
NG_032118.1:g.64606A>G , LRG_410:g.64606A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.679A>G	ENSP00000346369.2:p.Ile227Val
ENST00000373675.4:c.1504A>G	ENSP00000362779.4:p.Ile502Val
ENST00000540630.6:c.1558A>G	ENSP00000441668.3:p.Ile520Val
ENST00000613327.5:c.1504A>G	ENSP00000480757.2:p.Ile502Val
ENST00000687572.1:c.382A>G	ENSP00000510427.1:p.Ile128Val
ENST00000687705.1:c.*1753A>G	ENSP00000509639.1:n.*1753A>G
ENST00000688812.1:c.1480A>G	ENSP00000510658.1:p.Ile494Val
ENST00000689002.1:n.556A>G
ENST00000690544.1:c.*775A>G	ENSP00000508989.1:n.*775A>G
ENST00000358913.10:c.1504A>G MANE Select	ENSP00000351790.5:p.Ile502Val
ENST00000354393.6:c.679A>G	ENSP00000346369.2:p.Ile227Val
ENST00000358913.9:c.1504A>G	ENSP00000351790.5:p.Ile502Val
ENST00000540630.5:c.1504A>G	ENSP00000441668.2:p.Ile502Val
ENST00000613327.4:c.622A>G	ENSP00000480757.1:p.Ile208Val
NM_001256267.1:c.1504A>G	NP_001243196.1:p.Ile502Val
NM_001256268.1:c.622A>G	NP_001243197.1:p.Ile208Val
NM_032578.3:c.1504A>G , LRG_410t1:c.1504A>G	NP_115967.2:p.Ile502Val
NR_045662.3:n.931A>G
NR_045663.3:n.1772A>G
XM_006718043.2:c.1558A>G	XP_006718106.1:p.Ile520Val
XM_011540292.1:c.1534A>G	XP_011538594.1:p.Ile512Val
XM_017016833.1:c.1582A>G	XP_016872322.1:p.Ile528Val
XM_017016834.2:c.1504A>G	XP_016872323.1:p.Ile502Val
XM_024448236.1:c.382A>G	XP_024304004.1:p.Ile128Val
NR_045662.4:n.1041A>G
NR_045663.4:n.1717A>G
NM_001256267.2:c.1504A>G	NP_001243196.1:p.Ile502Val
NM_001256268.2:c.622A>G	NP_001243197.1:p.Ile208Val
NM_032578.4:c.1504A>G MANE Select	NP_115967.2:p.Ile502Val