Canonical Allele Identifier: CA376839305

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926060A>T (hg19) ; chr10:g.68166303A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166303A>T , CM000672.2:g.68166303A>T	GRCh38
NC_000010.10:g.69926060A>T , CM000672.1:g.69926060A>T	GRCh37
NC_000010.9:g.69596066A>T	NCBI36
NG_032118.1:g.65187A>T , LRG_410:g.65187A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.785A>T	ENSP00000346369.2:p.Asp262Val
ENST00000373675.4:c.1610A>T	ENSP00000362779.4:p.Asp537Val
ENST00000540630.6:c.1664A>T	ENSP00000441668.3:p.Asp555Val
ENST00000613327.5:c.1610A>T	ENSP00000480757.2:p.Asp537Val
ENST00000687572.1:c.488A>T	ENSP00000510427.1:p.Asp163Val
ENST00000687705.1:c.*1859A>T	ENSP00000509639.1:n.*1859A>T
ENST00000688812.1:c.1586A>T	ENSP00000510658.1:p.Asp529Val
ENST00000689002.1:n.662A>T
ENST00000690544.1:c.*881A>T	ENSP00000508989.1:n.*881A>T
ENST00000358913.10:c.1610A>T MANE Select	ENSP00000351790.5:p.Asp537Val
ENST00000354393.6:c.785A>T	ENSP00000346369.2:p.Asp262Val
ENST00000358913.9:c.1610A>T	ENSP00000351790.5:p.Asp537Val
ENST00000540630.5:c.1610A>T	ENSP00000441668.2:p.Asp537Val
ENST00000613327.4:c.728A>T	ENSP00000480757.1:p.Asp243Val
NM_001256267.1:c.1610A>T	NP_001243196.1:p.Asp537Val
NM_001256268.1:c.728A>T	NP_001243197.1:p.Asp243Val
NM_032578.3:c.1610A>T , LRG_410t1:c.1610A>T	NP_115967.2:p.Asp537Val
NR_045662.3:n.1037A>T
NR_045663.3:n.1878A>T
XM_006718043.2:c.1664A>T	XP_006718106.1:p.Asp555Val
XM_011540292.1:c.1640A>T	XP_011538594.1:p.Asp547Val
XM_017016833.1:c.1688A>T	XP_016872322.1:p.Asp563Val
XM_017016834.2:c.1610A>T	XP_016872323.1:p.Asp537Val
XM_024448236.1:c.488A>T	XP_024304004.1:p.Asp163Val
NR_045662.4:n.1147A>T
NR_045663.4:n.1823A>T
NM_001256267.2:c.1610A>T	NP_001243196.1:p.Asp537Val
NM_001256268.2:c.728A>T	NP_001243197.1:p.Asp243Val
NM_032578.4:c.1610A>T MANE Select	NP_115967.2:p.Asp537Val