Canonical Allele Identifier: CA482935847

Gene: MIPEP

Linked Data

• gnomAD v4: 13-23862344-C-T
• MyVariant Identifiers: chr13:g.24436483C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23862344C>T , CM000675.2:g.23862344C>T	GRCh38
NC_000013.10:g.24436483C>T , CM000675.1:g.24436483C>T	GRCh37
NC_000013.9:g.23334483C>T	NCBI36
NG_052977.1:g.32105G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382172.4:c.1011G>A MANE Select	ENSP00000371607.3:p.Glu337=
ENST00000382172.3:c.1011G>A	ENSP00000371607.3:p.Glu337=
ENST00000494139.1:n.408G>A
NM_005932.3:c.1011G>A	NP_005923.2:p.Glu337=
XM_011535097.1:c.825G>A	XP_011533399.1:p.Glu275=
XM_011535098.1:c.1011G>A	XP_011533400.1:p.Glu337=
XM_011535097.2:c.825G>A	XP_011533399.1:p.Glu275=
XM_011535098.3:c.1011G>A	XP_011533400.1:p.Glu337=
NM_005932.4:c.1011G>A MANE Select	NP_005923.3:p.Glu337=