Canonical Allele Identifier: CA5522641

Gene: MYPN

Linked Data

• ClinVar Variation Id: 1778123
• ClinVar RCV Id: RCV002414633
• dbSNP Id: rs756292351
• ExAC: 10:69926140 C / A
• gnomAD v2: 10-69926140-C-A
• gnomAD v3: 10-68166383-C-A
• gnomAD v4: 10-68166383-C-A
• MyVariant Identifiers: chr10:g.69926140C>A (hg19) ; chr10:g.68166383C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166383C>A , CM000672.2:g.68166383C>A	GRCh38
NC_000010.10:g.69926140C>A , CM000672.1:g.69926140C>A	GRCh37
NC_000010.9:g.69596146C>A	NCBI36
NG_032118.1:g.65267C>A , LRG_410:g.65267C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.865C>A	ENSP00000346369.2:p.His289Asn
ENST00000373675.4:c.1690C>A	ENSP00000362779.4:p.His564Asn
ENST00000540630.6:c.1744C>A	ENSP00000441668.3:p.His582Asn
ENST00000613327.5:c.1690C>A	ENSP00000480757.2:p.His564Asn
ENST00000687572.1:c.568C>A	ENSP00000510427.1:p.His190Asn
ENST00000688812.1:c.1666C>A	ENSP00000510658.1:p.His556Asn
ENST00000689002.1:n.742C>A
ENST00000690544.1:c.*961C>A	ENSP00000508989.1:n.*961C>A
ENST00000358913.10:c.1690C>A MANE Select	ENSP00000351790.5:p.His564Asn
ENST00000354393.6:c.865C>A	ENSP00000346369.2:p.His289Asn
ENST00000358913.9:c.1690C>A	ENSP00000351790.5:p.His564Asn
ENST00000540630.5:c.1690C>A	ENSP00000441668.2:p.His564Asn
ENST00000613327.4:c.808C>A	ENSP00000480757.1:p.His270Asn
NM_001256267.1:c.1690C>A	NP_001243196.1:p.His564Asn
NM_001256268.1:c.808C>A	NP_001243197.1:p.His270Asn
NM_032578.3:c.1690C>A , LRG_410t1:c.1690C>A	NP_115967.2:p.His564Asn
NR_045662.3:n.1117C>A
NR_045663.3:n.1958C>A
XM_006718043.2:c.1744C>A	XP_006718106.1:p.His582Asn
XM_011540292.1:c.1720C>A	XP_011538594.1:p.His574Asn
XM_017016833.1:c.1768C>A	XP_016872322.1:p.His590Asn
XM_017016834.2:c.1690C>A	XP_016872323.1:p.His564Asn
XM_024448236.1:c.568C>A	XP_024304004.1:p.His190Asn
NR_045662.4:n.1227C>A
NR_045663.4:n.1903C>A
NM_001256267.2:c.1690C>A	NP_001243196.1:p.His564Asn
NM_001256268.2:c.808C>A	NP_001243197.1:p.His270Asn
NM_032578.4:c.1690C>A MANE Select	NP_115967.2:p.His564Asn