Canonical Allele Identifier: CA482935855

Gene: MIPEP

Linked Data

• MyVariant Identifiers: chr13:g.24436498A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23862359A>C , CM000675.2:g.23862359A>C	GRCh38
NC_000013.10:g.24436498A>C , CM000675.1:g.24436498A>C	GRCh37
NC_000013.9:g.23334498A>C	NCBI36
NG_052977.1:g.32090T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382172.4:c.996T>G MANE Select	ENSP00000371607.3:p.Thr332=
ENST00000382172.3:c.996T>G	ENSP00000371607.3:p.Thr332=
ENST00000494139.1:n.393T>G
NM_005932.3:c.996T>G	NP_005923.2:p.Thr332=
XM_011535097.1:c.810T>G	XP_011533399.1:p.Thr270=
XM_011535098.1:c.996T>G	XP_011533400.1:p.Thr332=
XM_011535097.2:c.810T>G	XP_011533399.1:p.Thr270=
XM_011535098.3:c.996T>G	XP_011533400.1:p.Thr332=
NM_005932.4:c.996T>G MANE Select	NP_005923.3:p.Thr332=