Canonical Allele Identifier: CA482935741

Gene: MIPEP

Linked Data

• gnomAD v4: 13-23862311-A-G
• MyVariant Identifiers: chr13:g.24436450A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23862311A>G , CM000675.2:g.23862311A>G	GRCh38
NC_000013.10:g.24436450A>G , CM000675.1:g.24436450A>G	GRCh37
NC_000013.9:g.23334450A>G	NCBI36
NG_052977.1:g.32138T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382172.4:c.1044T>C MANE Select	ENSP00000371607.3:p.Pro348=
ENST00000382172.3:c.1044T>C	ENSP00000371607.3:p.Pro348=
ENST00000494139.1:n.441T>C
NM_005932.3:c.1044T>C	NP_005923.2:p.Pro348=
XM_011535097.1:c.858T>C	XP_011533399.1:p.Pro286=
XM_011535098.1:c.1044T>C	XP_011533400.1:p.Pro348=
XM_011535097.2:c.858T>C	XP_011533399.1:p.Pro286=
XM_011535098.3:c.1044T>C	XP_011533400.1:p.Pro348=
NM_005932.4:c.1044T>C MANE Select	NP_005923.3:p.Pro348=