Canonical Allele Identifier: CA376839465

Gene: MYPN

Linked Data

• gnomAD v4: 10-68166332-G-A
• MyVariant Identifiers: chr10:g.69926089G>A (hg19) ; chr10:g.68166332G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166332G>A , CM000672.2:g.68166332G>A	GRCh38
NC_000010.10:g.69926089G>A , CM000672.1:g.69926089G>A	GRCh37
NC_000010.9:g.69596095G>A	NCBI36
NG_032118.1:g.65216G>A , LRG_410:g.65216G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.814G>A	ENSP00000346369.2:p.Ala272Thr
ENST00000373675.4:c.1639G>A	ENSP00000362779.4:p.Ala547Thr
ENST00000540630.6:c.1693G>A	ENSP00000441668.3:p.Ala565Thr
ENST00000613327.5:c.1639G>A	ENSP00000480757.2:p.Ala547Thr
ENST00000687572.1:c.517G>A	ENSP00000510427.1:p.Ala173Thr
ENST00000687705.1:c.*1888G>A	ENSP00000509639.1:n.*1888G>A
ENST00000688812.1:c.1615G>A	ENSP00000510658.1:p.Ala539Thr
ENST00000689002.1:n.691G>A
ENST00000690544.1:c.*910G>A	ENSP00000508989.1:n.*910G>A
ENST00000358913.10:c.1639G>A MANE Select	ENSP00000351790.5:p.Ala547Thr
ENST00000354393.6:c.814G>A	ENSP00000346369.2:p.Ala272Thr
ENST00000358913.9:c.1639G>A	ENSP00000351790.5:p.Ala547Thr
ENST00000540630.5:c.1639G>A	ENSP00000441668.2:p.Ala547Thr
ENST00000613327.4:c.757G>A	ENSP00000480757.1:p.Ala253Thr
NM_001256267.1:c.1639G>A	NP_001243196.1:p.Ala547Thr
NM_001256268.1:c.757G>A	NP_001243197.1:p.Ala253Thr
NM_032578.3:c.1639G>A , LRG_410t1:c.1639G>A	NP_115967.2:p.Ala547Thr
NR_045662.3:n.1066G>A
NR_045663.3:n.1907G>A
XM_006718043.2:c.1693G>A	XP_006718106.1:p.Ala565Thr
XM_011540292.1:c.1669G>A	XP_011538594.1:p.Ala557Thr
XM_017016833.1:c.1717G>A	XP_016872322.1:p.Ala573Thr
XM_017016834.2:c.1639G>A	XP_016872323.1:p.Ala547Thr
XM_024448236.1:c.517G>A	XP_024304004.1:p.Ala173Thr
NR_045662.4:n.1176G>A
NR_045663.4:n.1852G>A
NM_001256267.2:c.1639G>A	NP_001243196.1:p.Ala547Thr
NM_001256268.2:c.757G>A	NP_001243197.1:p.Ala253Thr
NM_032578.4:c.1639G>A MANE Select	NP_115967.2:p.Ala547Thr