Canonical Allele Identifier: CA2609373126

Gene: MYPN

Linked Data

• gnomAD v4: 10-68195521-TCAGTCTCACAGGTAAAGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195526_68195543del , CM000672.2:g.68195526_68195543del	GRCh38
NC_000010.10:g.69955283_69955300del , CM000672.1:g.69955283_69955300del	GRCh37
NC_000010.9:g.69625289_69625306del	NCBI36
NG_032118.1:g.94410_94427del , LRG_410:g.94410_94427del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2327_2333+11del
ENST00000540630.6:c.3206_3212+11del
ENST00000613327.5:c.3152_3158+11del
ENST00000688812.1:c.*415_*421+11del
ENST00000690544.1:c.*2423_*2429+11del
ENST00000358913.10:c.3152_3158+11del
ENST00000354393.6:c.2327_2333+11del
ENST00000358913.9:c.3152_3158+11del
ENST00000540630.5:c.3152_3158+11del
ENST00000613327.4:c.2270_2276+11del
NM_001256267.1:c.3152_3158+11del
NM_001256268.1:c.2270_2276+11del
NM_032578.3:c.3152_3158+11del , LRG_410t1:c.3152_3158+11del
NR_045662.3:n.2579_2585+11del
NR_045663.3:n.3281_3287+11del
XM_006718043.2:c.3206_3212+11del
XM_011540292.1:c.3182_3188+11del
XM_017016833.1:c.3230_3236+11del
XM_017016834.2:c.3152_3158+11del
XM_024448236.1:c.2030_2036+11del
NR_045662.4:n.2689_2695+11del
NR_045663.4:n.3226_3232+11del
NM_001256267.2:c.3152_3158+11del
NM_001256268.2:c.2270_2276+11del
NM_032578.4:c.3152_3158+11del