Canonical Allele Identifier: CA376859281

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199501A>T , CM000672.2:g.68199501A>T	GRCh38
NC_000010.10:g.69959258A>T , CM000672.1:g.69959258A>T	GRCh37
NC_000010.9:g.69629264A>T	NCBI36
NG_032118.1:g.98385A>T , LRG_410:g.98385A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3419A>T MANE Select	NP_115967.2:p.Asp1140Val
ENST00000358913.10:c.3419A>T MANE Select	ENSP00000351790.5:p.Asp1140Val
NM_001256267.1:c.3419A>T	NP_001243196.1:p.Asp1140Val
NM_001256267.2:c.3419A>T	NP_001243196.1:p.Asp1140Val
NM_001256268.1:c.2537A>T	NP_001243197.1:p.Asp846Val
NM_001256268.2:c.2537A>T	NP_001243197.1:p.Asp846Val
NM_032578.3:c.3419A>T , LRG_410t1:c.3419A>T	NP_115967.2:p.Asp1140Val
NR_045662.3:n.2846A>T
NR_045662.4:n.2956A>T
NR_045663.3:n.3548A>T
NR_045663.4:n.3493A>T
ENST00000354393.6:c.2594A>T	ENSP00000346369.2:p.Asp865Val
ENST00000354393.7:c.2594A>T	ENSP00000346369.2:p.Asp865Val
ENST00000358913.9:c.3419A>T	ENSP00000351790.5:p.Asp1140Val
ENST00000540630.5:c.3419A>T	ENSP00000441668.2:p.Asp1140Val
ENST00000540630.6:c.3473A>T	ENSP00000441668.3:p.Asp1158Val
ENST00000613327.4:c.2537A>T	ENSP00000480757.1:p.Asp846Val
ENST00000613327.5:c.3419A>T	ENSP00000480757.2:p.Asp1140Val
ENST00000688812.1:c.*682A>T	ENSP00000510658.1:n.*682A>T
ENST00000690544.1:c.*2690A>T	ENSP00000508989.1:n.*2690A>T
XM_006718043.2:c.3473A>T	XP_006718106.1:p.Asp1158Val
XM_011540292.1:c.3449A>T	XP_011538594.1:p.Asp1150Val
XM_017016833.1:c.3497A>T	XP_016872322.1:p.Asp1166Val
XM_017016834.2:c.3419A>T	XP_016872323.1:p.Asp1140Val
XM_024448236.1:c.2297A>T	XP_024304004.1:p.Asp766Val
XR_946029.1:n.1804-226T>A