Canonical Allele Identifier: CA1917227394

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199423_68199425delinsTAC , CM000672.2:g.68199423_68199425delinsTAC	GRCh38
NC_000010.10:g.69959180_69959182delinsTAC , CM000672.1:g.69959180_69959182delinsTAC	GRCh37
NC_000010.9:g.69629186_69629188delinsTAC	NCBI36
NG_032118.1:g.98307_98309delinsTAC , LRG_410:g.98307_98309delinsTAC

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3341_3343delinsTAC MANE Select	NP_115967.2:p.Leu1114=
ENST00000358913.10:c.3341_3343delinsTAC MANE Select	ENSP00000351790.5:p.Leu1114=
NM_001256267.1:c.3341_3343delinsTAC	NP_001243196.1:p.Leu1114=
NM_001256267.2:c.3341_3343delinsTAC	NP_001243196.1:p.Leu1114=
NM_001256268.1:c.2459_2461delinsTAC	NP_001243197.1:p.Leu820=
NM_001256268.2:c.2459_2461delinsTAC	NP_001243197.1:p.Leu820=
NM_032578.3:c.3341_3343delinsTAC , LRG_410t1:c.3341_3343delinsTAC	NP_115967.2:p.Leu1114=
NR_045662.3:n.2768_2770delinsTAC
NR_045662.4:n.2878_2880delinsTAC
NR_045663.3:n.3470_3472delinsTAC
NR_045663.4:n.3415_3417delinsTAC
ENST00000354393.6:c.2516_2518delinsTAC	ENSP00000346369.2:p.Leu839=
ENST00000354393.7:c.2516_2518delinsTAC	ENSP00000346369.2:p.Leu839=
ENST00000358913.9:c.3341_3343delinsTAC	ENSP00000351790.5:p.Leu1114=
ENST00000540630.5:c.3341_3343delinsTAC	ENSP00000441668.2:p.Leu1114=
ENST00000540630.6:c.3395_3397delinsTAC	ENSP00000441668.3:p.Leu1132=
ENST00000613327.4:c.2459_2461delinsTAC	ENSP00000480757.1:p.Leu820=
ENST00000613327.5:c.3341_3343delinsTAC	ENSP00000480757.2:p.Leu1114=
ENST00000688812.1:c.*604_*606delinsTAC	ENSP00000510658.1:n.*604_*606delinsTAC
ENST00000690544.1:c.*2612_*2614delinsTAC	ENSP00000508989.1:n.*2612_*2614delinsTAC
XM_006718043.2:c.3395_3397delinsTAC	XP_006718106.1:p.Leu1132=
XM_011540292.1:c.3371_3373delinsTAC	XP_011538594.1:p.Leu1124=
XM_017016833.1:c.3419_3421delinsTAC	XP_016872322.1:p.Leu1140=
XM_017016834.2:c.3341_3343delinsTAC	XP_016872323.1:p.Leu1114=
XM_024448236.1:c.2219_2221delinsTAC	XP_024304004.1:p.Leu740=
XR_946029.1:n.1804-150_1804-148delinsGTA