Canonical Allele Identifier: CA387526145

Gene: MIPEP

Linked Data

• gnomAD v4: 13-23862341-C-T
• MyVariant Identifiers: chr13:g.24436480C>T (hg19) ; chr13:g.23862341C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23862341C>T , CM000675.2:g.23862341C>T	GRCh38
NC_000013.10:g.24436480C>T , CM000675.1:g.24436480C>T	GRCh37
NC_000013.9:g.23334480C>T	NCBI36
NG_052977.1:g.32108G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382172.4:c.1014G>A MANE Select	ENSP00000371607.3:p.Met338Ile
ENST00000382172.3:c.1014G>A	ENSP00000371607.3:p.Met338Ile
ENST00000494139.1:n.411G>A
NM_005932.3:c.1014G>A	NP_005923.2:p.Met338Ile
XM_011535097.1:c.828G>A	XP_011533399.1:p.Met276Ile
XM_011535098.1:c.1014G>A	XP_011533400.1:p.Met338Ile
XM_011535097.2:c.828G>A	XP_011533399.1:p.Met276Ile
XM_011535098.3:c.1014G>A	XP_011533400.1:p.Met338Ile
NM_005932.4:c.1014G>A MANE Select	NP_005923.3:p.Met338Ile