Canonical Allele Identifier: CA376839494

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926094C>G (hg19) ; chr10:g.68166337C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166337C>G , CM000672.2:g.68166337C>G	GRCh38
NC_000010.10:g.69926094C>G , CM000672.1:g.69926094C>G	GRCh37
NC_000010.9:g.69596100C>G	NCBI36
NG_032118.1:g.65221C>G , LRG_410:g.65221C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.819C>G	ENSP00000346369.2:p.Asn273Lys
ENST00000373675.4:c.1644C>G	ENSP00000362779.4:p.Asn548Lys
ENST00000540630.6:c.1698C>G	ENSP00000441668.3:p.Asn566Lys
ENST00000613327.5:c.1644C>G	ENSP00000480757.2:p.Asn548Lys
ENST00000687572.1:c.522C>G	ENSP00000510427.1:p.Asn174Lys
ENST00000687705.1:c.*1893C>G	ENSP00000509639.1:n.*1893C>G
ENST00000688812.1:c.1620C>G	ENSP00000510658.1:p.Asn540Lys
ENST00000689002.1:n.696C>G
ENST00000690544.1:c.*915C>G	ENSP00000508989.1:n.*915C>G
ENST00000358913.10:c.1644C>G MANE Select	ENSP00000351790.5:p.Asn548Lys
ENST00000354393.6:c.819C>G	ENSP00000346369.2:p.Asn273Lys
ENST00000358913.9:c.1644C>G	ENSP00000351790.5:p.Asn548Lys
ENST00000540630.5:c.1644C>G	ENSP00000441668.2:p.Asn548Lys
ENST00000613327.4:c.762C>G	ENSP00000480757.1:p.Asn254Lys
NM_001256267.1:c.1644C>G	NP_001243196.1:p.Asn548Lys
NM_001256268.1:c.762C>G	NP_001243197.1:p.Asn254Lys
NM_032578.3:c.1644C>G , LRG_410t1:c.1644C>G	NP_115967.2:p.Asn548Lys
NR_045662.3:n.1071C>G
NR_045663.3:n.1912C>G
XM_006718043.2:c.1698C>G	XP_006718106.1:p.Asn566Lys
XM_011540292.1:c.1674C>G	XP_011538594.1:p.Asn558Lys
XM_017016833.1:c.1722C>G	XP_016872322.1:p.Asn574Lys
XM_017016834.2:c.1644C>G	XP_016872323.1:p.Asn548Lys
XM_024448236.1:c.522C>G	XP_024304004.1:p.Asn174Lys
NR_045662.4:n.1181C>G
NR_045663.4:n.1857C>G
NM_001256267.2:c.1644C>G	NP_001243196.1:p.Asn548Lys
NM_001256268.2:c.762C>G	NP_001243197.1:p.Asn254Lys
NM_032578.4:c.1644C>G MANE Select	NP_115967.2:p.Asn548Lys