Canonical Allele Identifier: CA1917226393

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68197269_68197270delinsCT , CM000672.2:g.68197269_68197270delinsCT	GRCh38
NC_000010.10:g.69957026_69957027delinsCT , CM000672.1:g.69957026_69957027delinsCT	GRCh37
NC_000010.9:g.69627032_69627033delinsCT	NCBI36
NG_032118.1:g.96153_96154delinsCT , LRG_410:g.96153_96154delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2334-83_2334-82delinsCT	ENSP00000346369.2:n.2334-83_2334-82delinsCT
ENST00000540630.6:c.3213-83_3213-82delinsCT	ENSP00000441668.3:n.3213-83_3213-82delinsCT
ENST00000613327.5:c.3159-83_3159-82delinsCT	ENSP00000480757.2:n.3159-83_3159-82delinsCT
ENST00000688812.1:c.*422-83_*422-82delinsCT	ENSP00000510658.1:n.*422-83_*422-82delinsCT
ENST00000690544.1:c.*2430-83_*2430-82delinsCT	ENSP00000508989.1:n.*2430-83_*2430-82delinsCT
ENST00000358913.10:c.3159-83_3159-82delinsCT MANE Select	ENSP00000351790.5:n.3159-83_3159-82delinsCT
ENST00000354393.6:c.2334-83_2334-82delinsCT	ENSP00000346369.2:n.2334-83_2334-82delinsCT
ENST00000358913.9:c.3159-83_3159-82delinsCT	ENSP00000351790.5:n.3159-83_3159-82delinsCT
ENST00000540630.5:c.3159-83_3159-82delinsCT	ENSP00000441668.2:n.3159-83_3159-82delinsCT
ENST00000613327.4:c.2277-83_2277-82delinsCT	ENSP00000480757.1:n.2277-83_2277-82delinsCT
NM_001256267.1:c.3159-83_3159-82delinsCT	NP_001243196.1:n.3159-83_3159-82delinsCT
NM_001256268.1:c.2277-83_2277-82delinsCT	NP_001243197.1:n.2277-83_2277-82delinsCT
NM_032578.3:c.3159-83_3159-82delinsCT , LRG_410t1:c.3159-83_3159-82delinsCT	NP_115967.2:n.3159-83_3159-82delinsCT
NR_045662.3:n.2586-83_2586-82delinsCT
NR_045663.3:n.3288-83_3288-82delinsCT
XM_006718043.2:c.3213-83_3213-82delinsCT	XP_006718106.1:n.3213-83_3213-82delinsCT
XM_011540292.1:c.3189-83_3189-82delinsCT	XP_011538594.1:n.3189-83_3189-82delinsCT
XM_017016833.1:c.3237-83_3237-82delinsCT	XP_016872322.1:n.3237-83_3237-82delinsCT
XM_017016834.2:c.3159-83_3159-82delinsCT	XP_016872323.1:n.3159-83_3159-82delinsCT
XM_024448236.1:c.2037-83_2037-82delinsCT	XP_024304004.1:n.2037-83_2037-82delinsCT
NR_045662.4:n.2696-83_2696-82delinsCT
NR_045663.4:n.3233-83_3233-82delinsCT
NM_001256267.2:c.3159-83_3159-82delinsCT	NP_001243196.1:n.3159-83_3159-82delinsCT
NM_001256268.2:c.2277-83_2277-82delinsCT	NP_001243197.1:n.2277-83_2277-82delinsCT
NM_032578.4:c.3159-83_3159-82delinsCT MANE Select	NP_115967.2:n.3159-83_3159-82delinsCT