Canonical Allele Identifier: CA376859304

Gene: MYPN

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3430T>C MANE Select	NP_115967.2:p.Tyr1144His
ENST00000358913.10:c.3430T>C MANE Select	ENSP00000351790.5:p.Tyr1144His
NM_001256267.1:c.3430T>C	NP_001243196.1:p.Tyr1144His
NM_001256267.2:c.3430T>C	NP_001243196.1:p.Tyr1144His
NM_001256268.1:c.2548T>C	NP_001243197.1:p.Tyr850His
NM_001256268.2:c.2548T>C	NP_001243197.1:p.Tyr850His
NM_032578.3:c.3430T>C , LRG_410t1:c.3430T>C	NP_115967.2:p.Tyr1144His
NR_045662.3:n.2857T>C
NR_045662.4:n.2967T>C
NR_045663.3:n.3559T>C
NR_045663.4:n.3504T>C
ENST00000354393.6:c.2605T>C	ENSP00000346369.2:p.Tyr869His
ENST00000354393.7:c.2605T>C	ENSP00000346369.2:p.Tyr869His
ENST00000358913.9:c.3430T>C	ENSP00000351790.5:p.Tyr1144His
ENST00000540630.5:c.3430T>C	ENSP00000441668.2:p.Tyr1144His
ENST00000540630.6:c.3484T>C	ENSP00000441668.3:p.Tyr1162His
ENST00000613327.4:c.2548T>C	ENSP00000480757.1:p.Tyr850His
ENST00000613327.5:c.3430T>C	ENSP00000480757.2:p.Tyr1144His
ENST00000688812.1:c.*693T>C	ENSP00000510658.1:n.*693T>C
ENST00000690544.1:c.*2701T>C	ENSP00000508989.1:n.*2701T>C
XM_006718043.2:c.3484T>C	XP_006718106.1:p.Tyr1162His
XM_011540292.1:c.3460T>C	XP_011538594.1:p.Tyr1154His
XM_017016833.1:c.3508T>C	XP_016872322.1:p.Tyr1170His
XM_017016834.2:c.3430T>C	XP_016872323.1:p.Tyr1144His
XM_024448236.1:c.2308T>C	XP_024304004.1:p.Tyr770His
XR_946029.1:n.1804-237A>G