Canonical Allele Identifier: CA2580081725

Gene: MYPN

Linked Data

• ClinVar Variation Id: 1878937
• ClinVar RCV Id: RCV002511438
• gnomAD v4: 10-68166409-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166415dup , CM000672.2:g.68166415dup	GRCh38
NC_000010.10:g.69926172dup , CM000672.1:g.69926172dup	GRCh37
NC_000010.9:g.69596178dup	NCBI36
NG_032118.1:g.65299dup , LRG_410:g.65299dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.897dup	ENSP00000346369.2:p.Lys300GlnfsTer13
ENST00000373675.4:c.1722dup	ENSP00000362779.4:p.Lys575GlnfsTer13
ENST00000540630.6:c.1776dup	ENSP00000441668.3:p.Lys593GlnfsTer13
ENST00000613327.5:c.1722dup	ENSP00000480757.2:p.Lys575GlnfsTer13
ENST00000687572.1:c.600dup	ENSP00000510427.1:p.Lys201GlnfsTer13
ENST00000688812.1:c.1698dup	ENSP00000510658.1:p.Lys567GlnfsTer13
ENST00000689002.1:n.774dup
ENST00000690544.1:c.*993dup	ENSP00000508989.1:n.*993dup
ENST00000358913.10:c.1722dup MANE Select	ENSP00000351790.5:p.Lys575GlnfsTer13
ENST00000354393.6:c.897dup	ENSP00000346369.2:p.Lys300GlnfsTer13
ENST00000358913.9:c.1722dup	ENSP00000351790.5:p.Lys575GlnfsTer13
ENST00000540630.5:c.1722dup	ENSP00000441668.2:p.Lys575GlnfsTer13
ENST00000613327.4:c.840dup	ENSP00000480757.1:p.Lys281GlnfsTer13
NM_001256267.1:c.1722dup	NP_001243196.1:p.Lys575GlnfsTer13
NM_001256268.1:c.840dup	NP_001243197.1:p.Lys281GlnfsTer13
NM_032578.3:c.1722dup , LRG_410t1:c.1722dup	NP_115967.2:p.Lys575GlnfsTer13
NR_045662.3:n.1149dup
NR_045663.3:n.1990dup
XM_006718043.2:c.1776dup	XP_006718106.1:p.Lys593GlnfsTer13
XM_011540292.1:c.1752dup	XP_011538594.1:p.Lys585GlnfsTer13
XM_017016833.1:c.1800dup	XP_016872322.1:p.Lys601GlnfsTer13
XM_017016834.2:c.1722dup	XP_016872323.1:p.Lys575GlnfsTer13
XM_024448236.1:c.600dup	XP_024304004.1:p.Lys201GlnfsTer13
NR_045662.4:n.1259dup
NR_045663.4:n.1935dup
NM_001256267.2:c.1722dup	NP_001243196.1:p.Lys575GlnfsTer13
NM_001256268.2:c.840dup	NP_001243197.1:p.Lys281GlnfsTer13
NM_032578.4:c.1722dup MANE Select	NP_115967.2:p.Lys575GlnfsTer13