Canonical Allele Identifier: CA2078857899

Gene: MIPEP

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23862347A= , CM000675.2:g.23862347A=	GRCh38
NC_000013.10:g.24436486A= , CM000675.1:g.24436486A=	GRCh37
NC_000013.9:g.23334486A=	NCBI36
NG_052977.1:g.32102T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382172.4:c.1008T= MANE Select	ENSP00000371607.3:p.Phe336=
ENST00000382172.3:c.1008T=	ENSP00000371607.3:p.Phe336=
ENST00000494139.1:n.405T=
NM_005932.3:c.1008T=	NP_005923.2:p.Phe336=
XM_011535097.1:c.822T=	XP_011533399.1:p.Phe274=
XM_011535098.1:c.1008T=	XP_011533400.1:p.Phe336=
XM_011535097.2:c.822T=	XP_011533399.1:p.Phe274=
XM_011535098.3:c.1008T=	XP_011533400.1:p.Phe336=
NM_005932.4:c.1008T= MANE Select	NP_005923.3:p.Phe336=