Canonical Allele Identifier: CA376838295

Gene: MYPN

Linked Data

• gnomAD v4: 10-68165775-C-G
• MyVariant Identifiers: chr10:g.69925532C>G (hg19) ; chr10:g.68165775C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165775C>G , CM000672.2:g.68165775C>G	GRCh38
NC_000010.10:g.69925532C>G , CM000672.1:g.69925532C>G	GRCh37
NC_000010.9:g.69595538C>G	NCBI36
NG_032118.1:g.64659C>G , LRG_410:g.64659C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.732C>G	ENSP00000346369.2:p.Asn244Lys
ENST00000373675.4:c.1557C>G	ENSP00000362779.4:p.Asn519Lys
ENST00000540630.6:c.1611C>G	ENSP00000441668.3:p.Asn537Lys
ENST00000613327.5:c.1557C>G	ENSP00000480757.2:p.Asn519Lys
ENST00000687572.1:c.435C>G	ENSP00000510427.1:p.Asn145Lys
ENST00000687705.1:c.*1806C>G	ENSP00000509639.1:n.*1806C>G
ENST00000688812.1:c.1533C>G	ENSP00000510658.1:p.Asn511Lys
ENST00000689002.1:n.609C>G
ENST00000690544.1:c.*828C>G	ENSP00000508989.1:n.*828C>G
ENST00000358913.10:c.1557C>G MANE Select	ENSP00000351790.5:p.Asn519Lys
ENST00000354393.6:c.732C>G	ENSP00000346369.2:p.Asn244Lys
ENST00000358913.9:c.1557C>G	ENSP00000351790.5:p.Asn519Lys
ENST00000540630.5:c.1557C>G	ENSP00000441668.2:p.Asn519Lys
ENST00000613327.4:c.675C>G	ENSP00000480757.1:p.Asn225Lys
NM_001256267.1:c.1557C>G	NP_001243196.1:p.Asn519Lys
NM_001256268.1:c.675C>G	NP_001243197.1:p.Asn225Lys
NM_032578.3:c.1557C>G , LRG_410t1:c.1557C>G	NP_115967.2:p.Asn519Lys
NR_045662.3:n.984C>G
NR_045663.3:n.1825C>G
XM_006718043.2:c.1611C>G	XP_006718106.1:p.Asn537Lys
XM_011540292.1:c.1587C>G	XP_011538594.1:p.Asn529Lys
XM_017016833.1:c.1635C>G	XP_016872322.1:p.Asn545Lys
XM_017016834.2:c.1557C>G	XP_016872323.1:p.Asn519Lys
XM_024448236.1:c.435C>G	XP_024304004.1:p.Asn145Lys
NR_045662.4:n.1094C>G
NR_045663.4:n.1770C>G
NM_001256267.2:c.1557C>G	NP_001243196.1:p.Asn519Lys
NM_001256268.2:c.675C>G	NP_001243197.1:p.Asn225Lys
NM_032578.4:c.1557C>G MANE Select	NP_115967.2:p.Asn519Lys