Canonical Allele Identifier: CA1917232486

Gene: MYPN

Linked Data

• dbSNP Id: rs2043894690

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210501_68210502insC , CM000672.2:g.68210501_68210502insC	GRCh38
NC_000010.10:g.69970258_69970259insC , CM000672.1:g.69970258_69970259insC	GRCh37
NC_000010.9:g.69640264_69640265insC	NCBI36
NG_032118.1:g.109385_109386insC , LRG_410:g.109385_109386insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.*46_*47insC	ENSP00000346369.2:n.*46_*47insC
ENST00000540630.6:c.*46_*47insC	ENSP00000441668.3:n.*46_*47insC
ENST00000613327.5:c.*46_*47insC	ENSP00000480757.2:n.*46_*47insC
ENST00000688812.1:c.*1272_*1273insC	ENSP00000510658.1:n.*1272_*1273insC
ENST00000690544.1:c.*3280_*3281insC	ENSP00000508989.1:n.*3280_*3281insC
ENST00000358913.10:c.*46_*47insC MANE Select	ENSP00000351790.5:n.*46_*47insC
ENST00000354393.6:c.*46_*47insC	ENSP00000346369.2:n.*46_*47insC
ENST00000358913.9:c.*46_*47insC	ENSP00000351790.5:n.*46_*47insC
ENST00000540630.5:c.*46_*47insC	ENSP00000441668.2:n.*46_*47insC
ENST00000613327.4:c.*46_*47insC	ENSP00000480757.1:n.*46_*47insC
NM_001256267.1:c.*46_*47insC	NP_001243196.1:n.*46_*47insC
NM_001256268.1:c.*46_*47insC	NP_001243197.1:n.*46_*47insC
NM_032578.3:c.*46_*47insC , LRG_410t1:c.*46_*47insC	NP_115967.2:n.*46_*47insC
NR_045662.3:n.3436_3437insC
NR_045663.3:n.4138_4139insC
XM_006718043.2:c.*46_*47insC	XP_006718106.1:n.*46_*47insC
XM_011540292.1:c.*46_*47insC	XP_011538594.1:n.*46_*47insC
XR_946029.1:n.1574+4786_1574+4787insG
XM_017016833.1:c.*46_*47insC	XP_016872322.1:n.*46_*47insC
XM_017016834.2:c.*46_*47insC	XP_016872323.1:n.*46_*47insC
XM_024448236.1:c.*46_*47insC	XP_024304004.1:n.*46_*47insC
NR_045662.4:n.3546_3547insC
NR_045663.4:n.4083_4084insC
NM_001256267.2:c.*46_*47insC	NP_001243196.1:n.*46_*47insC
NM_001256268.2:c.*46_*47insC	NP_001243197.1:n.*46_*47insC
NM_032578.4:c.*46_*47insC MANE Select	NP_115967.2:n.*46_*47insC