Canonical Allele Identifier: CA387525992

Gene: MIPEP

Linked Data

• gnomAD v4: 13-23862303-G-T
• MyVariant Identifiers: chr13:g.24436442G>T (hg19) ; chr13:g.23862303G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23862303G>T , CM000675.2:g.23862303G>T	GRCh38
NC_000013.10:g.24436442G>T , CM000675.1:g.24436442G>T	GRCh37
NC_000013.9:g.23334442G>T	NCBI36
NG_052977.1:g.32146C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382172.4:c.1052C>A MANE Select	ENSP00000371607.3:p.Ser351Tyr
ENST00000382172.3:c.1052C>A	ENSP00000371607.3:p.Ser351Tyr
ENST00000494139.1:n.449C>A
NM_005932.3:c.1052C>A	NP_005923.2:p.Ser351Tyr
XM_011535097.1:c.866C>A	XP_011533399.1:p.Ser289Tyr
XM_011535098.1:c.1052C>A	XP_011533400.1:p.Ser351Tyr
XM_011535097.2:c.866C>A	XP_011533399.1:p.Ser289Tyr
XM_011535098.3:c.1052C>A	XP_011533400.1:p.Ser351Tyr
NM_005932.4:c.1052C>A MANE Select	NP_005923.3:p.Ser351Tyr