Canonical Allele Identifier: CA2575370342

Gene: MIPEP

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23862416A>G , CM000675.2:g.23862416A>G	GRCh38
NC_000013.10:g.24436555A>G , CM000675.1:g.24436555A>G	GRCh37
NC_000013.9:g.23334555A>G	NCBI36
NG_052977.1:g.32033T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382172.4:c.993-54T>C MANE Select	ENSP00000371607.3:n.993-54T>C
ENST00000382172.3:c.993-54T>C	ENSP00000371607.3:n.993-54T>C
ENST00000494139.1:n.390-54T>C
NM_005932.3:c.993-54T>C	NP_005923.2:n.993-54T>C
XM_011535097.1:c.807-54T>C	XP_011533399.1:n.807-54T>C
XM_011535098.1:c.993-54T>C	XP_011533400.1:n.993-54T>C
XM_011535097.2:c.807-54T>C	XP_011533399.1:n.807-54T>C
XM_011535098.3:c.993-54T>C	XP_011533400.1:n.993-54T>C
NM_005932.4:c.993-54T>C MANE Select	NP_005923.3:n.993-54T>C