Canonical Allele Identifier: CA387526103

Gene: MIPEP

Linked Data

• MyVariant Identifiers: chr13:g.24436469A>G (hg19) ; chr13:g.23862330A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23862330A>G , CM000675.2:g.23862330A>G	GRCh38
NC_000013.10:g.24436469A>G , CM000675.1:g.24436469A>G	GRCh37
NC_000013.9:g.23334469A>G	NCBI36
NG_052977.1:g.32119T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382172.4:c.1025T>C MANE Select	ENSP00000371607.3:p.Met342Thr
ENST00000382172.3:c.1025T>C	ENSP00000371607.3:p.Met342Thr
ENST00000494139.1:n.422T>C
NM_005932.3:c.1025T>C	NP_005923.2:p.Met342Thr
XM_011535097.1:c.839T>C	XP_011533399.1:p.Met280Thr
XM_011535098.1:c.1025T>C	XP_011533400.1:p.Met342Thr
XM_011535097.2:c.839T>C	XP_011533399.1:p.Met280Thr
XM_011535098.3:c.1025T>C	XP_011533400.1:p.Met342Thr
NM_005932.4:c.1025T>C MANE Select	NP_005923.3:p.Met342Thr