Canonical Allele Identifier: CA376859303

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199512T>A , CM000672.2:g.68199512T>A	GRCh38
NC_000010.10:g.69959269T>A , CM000672.1:g.69959269T>A	GRCh37
NC_000010.9:g.69629275T>A	NCBI36
NG_032118.1:g.98396T>A , LRG_410:g.98396T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3430T>A MANE Select	NP_115967.2:p.Tyr1144Asn
ENST00000358913.10:c.3430T>A MANE Select	ENSP00000351790.5:p.Tyr1144Asn
NM_001256267.1:c.3430T>A	NP_001243196.1:p.Tyr1144Asn
NM_001256267.2:c.3430T>A	NP_001243196.1:p.Tyr1144Asn
NM_001256268.1:c.2548T>A	NP_001243197.1:p.Tyr850Asn
NM_001256268.2:c.2548T>A	NP_001243197.1:p.Tyr850Asn
NM_032578.3:c.3430T>A , LRG_410t1:c.3430T>A	NP_115967.2:p.Tyr1144Asn
NR_045662.3:n.2857T>A
NR_045662.4:n.2967T>A
NR_045663.3:n.3559T>A
NR_045663.4:n.3504T>A
ENST00000354393.6:c.2605T>A	ENSP00000346369.2:p.Tyr869Asn
ENST00000354393.7:c.2605T>A	ENSP00000346369.2:p.Tyr869Asn
ENST00000358913.9:c.3430T>A	ENSP00000351790.5:p.Tyr1144Asn
ENST00000540630.5:c.3430T>A	ENSP00000441668.2:p.Tyr1144Asn
ENST00000540630.6:c.3484T>A	ENSP00000441668.3:p.Tyr1162Asn
ENST00000613327.4:c.2548T>A	ENSP00000480757.1:p.Tyr850Asn
ENST00000613327.5:c.3430T>A	ENSP00000480757.2:p.Tyr1144Asn
ENST00000688812.1:c.*693T>A	ENSP00000510658.1:n.*693T>A
ENST00000690544.1:c.*2701T>A	ENSP00000508989.1:n.*2701T>A
XM_006718043.2:c.3484T>A	XP_006718106.1:p.Tyr1162Asn
XM_011540292.1:c.3460T>A	XP_011538594.1:p.Tyr1154Asn
XM_017016833.1:c.3508T>A	XP_016872322.1:p.Tyr1170Asn
XM_017016834.2:c.3430T>A	XP_016872323.1:p.Tyr1144Asn
XM_024448236.1:c.2308T>A	XP_024304004.1:p.Tyr770Asn
XR_946029.1:n.1804-237A>T