Canonical Allele Identifier: CA376839436

Gene: MYPN

Linked Data

• gnomAD v4: 10-68166326-C-A
• MyVariant Identifiers: chr10:g.69926083C>A (hg19) ; chr10:g.68166326C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166326C>A , CM000672.2:g.68166326C>A	GRCh38
NC_000010.10:g.69926083C>A , CM000672.1:g.69926083C>A	GRCh37
NC_000010.9:g.69596089C>A	NCBI36
NG_032118.1:g.65210C>A , LRG_410:g.65210C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.808C>A	ENSP00000346369.2:p.His270Asn
ENST00000373675.4:c.1633C>A	ENSP00000362779.4:p.His545Asn
ENST00000540630.6:c.1687C>A	ENSP00000441668.3:p.His563Asn
ENST00000613327.5:c.1633C>A	ENSP00000480757.2:p.His545Asn
ENST00000687572.1:c.511C>A	ENSP00000510427.1:p.His171Asn
ENST00000687705.1:c.*1882C>A	ENSP00000509639.1:n.*1882C>A
ENST00000688812.1:c.1609C>A	ENSP00000510658.1:p.His537Asn
ENST00000689002.1:n.685C>A
ENST00000690544.1:c.*904C>A	ENSP00000508989.1:n.*904C>A
ENST00000358913.10:c.1633C>A MANE Select	ENSP00000351790.5:p.His545Asn
ENST00000354393.6:c.808C>A	ENSP00000346369.2:p.His270Asn
ENST00000358913.9:c.1633C>A	ENSP00000351790.5:p.His545Asn
ENST00000540630.5:c.1633C>A	ENSP00000441668.2:p.His545Asn
ENST00000613327.4:c.751C>A	ENSP00000480757.1:p.His251Asn
NM_001256267.1:c.1633C>A	NP_001243196.1:p.His545Asn
NM_001256268.1:c.751C>A	NP_001243197.1:p.His251Asn
NM_032578.3:c.1633C>A , LRG_410t1:c.1633C>A	NP_115967.2:p.His545Asn
NR_045662.3:n.1060C>A
NR_045663.3:n.1901C>A
XM_006718043.2:c.1687C>A	XP_006718106.1:p.His563Asn
XM_011540292.1:c.1663C>A	XP_011538594.1:p.His555Asn
XM_017016833.1:c.1711C>A	XP_016872322.1:p.His571Asn
XM_017016834.2:c.1633C>A	XP_016872323.1:p.His545Asn
XM_024448236.1:c.511C>A	XP_024304004.1:p.His171Asn
NR_045662.4:n.1170C>A
NR_045663.4:n.1846C>A
NM_001256267.2:c.1633C>A	NP_001243196.1:p.His545Asn
NM_001256268.2:c.751C>A	NP_001243197.1:p.His251Asn
NM_032578.4:c.1633C>A MANE Select	NP_115967.2:p.His545Asn