Canonical Allele Identifier: CA469805683

Gene: MYPN

Linked Data

• gnomAD v4: 10-68166352-G-A
• MyVariant Identifiers: chr10:g.69926109G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166352G>A , CM000672.2:g.68166352G>A	GRCh38
NC_000010.10:g.69926109G>A , CM000672.1:g.69926109G>A	GRCh37
NC_000010.9:g.69596115G>A	NCBI36
NG_032118.1:g.65236G>A , LRG_410:g.65236G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.834G>A	ENSP00000346369.2:p.Leu278=
ENST00000373675.4:c.1659G>A	ENSP00000362779.4:p.Leu553=
ENST00000540630.6:c.1713G>A	ENSP00000441668.3:p.Leu571=
ENST00000613327.5:c.1659G>A	ENSP00000480757.2:p.Leu553=
ENST00000687572.1:c.537G>A	ENSP00000510427.1:p.Leu179=
ENST00000687705.1:c.*1908G>A	ENSP00000509639.1:n.*1908G>A
ENST00000688812.1:c.1635G>A	ENSP00000510658.1:p.Leu545=
ENST00000689002.1:n.711G>A
ENST00000690544.1:c.*930G>A	ENSP00000508989.1:n.*930G>A
ENST00000358913.10:c.1659G>A MANE Select	ENSP00000351790.5:p.Leu553=
ENST00000354393.6:c.834G>A	ENSP00000346369.2:p.Leu278=
ENST00000358913.9:c.1659G>A	ENSP00000351790.5:p.Leu553=
ENST00000540630.5:c.1659G>A	ENSP00000441668.2:p.Leu553=
ENST00000613327.4:c.777G>A	ENSP00000480757.1:p.Leu259=
NM_001256267.1:c.1659G>A	NP_001243196.1:p.Leu553=
NM_001256268.1:c.777G>A	NP_001243197.1:p.Leu259=
NM_032578.3:c.1659G>A , LRG_410t1:c.1659G>A	NP_115967.2:p.Leu553=
NR_045662.3:n.1086G>A
NR_045663.3:n.1927G>A
XM_006718043.2:c.1713G>A	XP_006718106.1:p.Leu571=
XM_011540292.1:c.1689G>A	XP_011538594.1:p.Leu563=
XM_017016833.1:c.1737G>A	XP_016872322.1:p.Leu579=
XM_017016834.2:c.1659G>A	XP_016872323.1:p.Leu553=
XM_024448236.1:c.537G>A	XP_024304004.1:p.Leu179=
NR_045662.4:n.1196G>A
NR_045663.4:n.1872G>A
NM_001256267.2:c.1659G>A	NP_001243196.1:p.Leu553=
NM_001256268.2:c.777G>A	NP_001243197.1:p.Leu259=
NM_032578.4:c.1659G>A MANE Select	NP_115967.2:p.Leu553=