Canonical Allele Identifier: CA2078857791

Gene: MIPEP

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23862300_23862301delinsAC , CM000675.2:g.23862300_23862301delinsAC	GRCh38
NC_000013.10:g.24436439_24436440delinsAC , CM000675.1:g.24436439_24436440delinsAC	GRCh37
NC_000013.9:g.23334439_23334440delinsAC	NCBI36
NG_052977.1:g.32148_32149delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382172.4:c.1053+1_1053+2delinsGT MANE Select	ENSP00000371607.3:n.1053+1_1053+2delinsGT
ENST00000382172.3:c.1053+1_1053+2delinsGT	ENSP00000371607.3:n.1053+1_1053+2delinsGT
ENST00000494139.1:n.450+1_450+2delinsGT
NM_005932.3:c.1053+1_1053+2delinsGT	NP_005923.2:n.1053+1_1053+2delinsGT
XM_011535097.1:c.867+1_867+2delinsGT	XP_011533399.1:n.867+1_867+2delinsGT
XM_011535098.1:c.1053+1_1053+2delinsGT	XP_011533400.1:n.1053+1_1053+2delinsGT
XM_011535097.2:c.867+1_867+2delinsGT	XP_011533399.1:n.867+1_867+2delinsGT
XM_011535098.3:c.1053+1_1053+2delinsGT	XP_011533400.1:n.1053+1_1053+2delinsGT
NM_005932.4:c.1053+1_1053+2delinsGT MANE Select	NP_005923.3:n.1053+1_1053+2delinsGT