Canonical Allele Identifier: CA376840589

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926327A>T (hg19) ; chr10:g.68166570A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166570A>T , CM000672.2:g.68166570A>T	GRCh38
NC_000010.10:g.69926327A>T , CM000672.1:g.69926327A>T	GRCh37
NC_000010.9:g.69596333A>T	NCBI36
NG_032118.1:g.65454A>T , LRG_410:g.65454A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1052A>T	ENSP00000346369.2:p.Asp351Val
ENST00000373675.4:c.1877A>T	ENSP00000362779.4:p.Asp626Val
ENST00000540630.6:c.1931A>T	ENSP00000441668.3:p.Asp644Val
ENST00000613327.5:c.1877A>T	ENSP00000480757.2:p.Asp626Val
ENST00000687572.1:c.755A>T	ENSP00000510427.1:p.Asp252Val
ENST00000688812.1:c.1853A>T	ENSP00000510658.1:p.Asp618Val
ENST00000690544.1:c.*1148A>T	ENSP00000508989.1:n.*1148A>T
ENST00000358913.10:c.1877A>T MANE Select	ENSP00000351790.5:p.Asp626Val
ENST00000354393.6:c.1052A>T	ENSP00000346369.2:p.Asp351Val
ENST00000358913.9:c.1877A>T	ENSP00000351790.5:p.Asp626Val
ENST00000540630.5:c.1877A>T	ENSP00000441668.2:p.Asp626Val
ENST00000613327.4:c.995A>T	ENSP00000480757.1:p.Asp332Val
NM_001256267.1:c.1877A>T	NP_001243196.1:p.Asp626Val
NM_001256268.1:c.995A>T	NP_001243197.1:p.Asp332Val
NM_032578.3:c.1877A>T , LRG_410t1:c.1877A>T	NP_115967.2:p.Asp626Val
NR_045662.3:n.1304A>T
NR_045663.3:n.2145A>T
XM_006718043.2:c.1931A>T	XP_006718106.1:p.Asp644Val
XM_011540292.1:c.1907A>T	XP_011538594.1:p.Asp636Val
XM_017016833.1:c.1955A>T	XP_016872322.1:p.Asp652Val
XM_017016834.2:c.1877A>T	XP_016872323.1:p.Asp626Val
XM_024448236.1:c.755A>T	XP_024304004.1:p.Asp252Val
NR_045662.4:n.1414A>T
NR_045663.4:n.2090A>T
NM_001256267.2:c.1877A>T	NP_001243196.1:p.Asp626Val
NM_001256268.2:c.995A>T	NP_001243197.1:p.Asp332Val
NM_032578.4:c.1877A>T MANE Select	NP_115967.2:p.Asp626Val