Canonical Allele Identifier: CA2078857847

Gene: MIPEP

Linked Data

• dbSNP Id: rs1870344455
• gnomAD v4: 13-23862316-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23862317_23862318del , CM000675.2:g.23862317_23862318del	GRCh38
NC_000013.10:g.24436456_24436457del , CM000675.1:g.24436456_24436457del	GRCh37
NC_000013.9:g.23334456_23334457del	NCBI36
NG_052977.1:g.32131_32132del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382172.4:c.1037_1038del MANE Select	ENSP00000371607.3:p.Leu346GlnfsTer25
ENST00000382172.3:c.1037_1038del	ENSP00000371607.3:p.Leu346GlnfsTer25
ENST00000494139.1:n.434_435del
NM_005932.3:c.1037_1038del	NP_005923.2:p.Leu346GlnfsTer25
XM_011535097.1:c.851_852del	XP_011533399.1:p.Leu284GlnfsTer25
XM_011535098.1:c.1037_1038del	XP_011533400.1:p.Leu346GlnfsTer25
XM_011535097.2:c.851_852del	XP_011533399.1:p.Leu284GlnfsTer25
XM_011535098.3:c.1037_1038del	XP_011533400.1:p.Leu346GlnfsTer25
NM_005932.4:c.1037_1038del MANE Select	NP_005923.3:p.Leu346GlnfsTer25