Canonical Allele Identifier: CA2561115538

Gene: MIPEP

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23862230C>T , CM000675.2:g.23862230C>T	GRCh38
NC_000013.10:g.24436369C>T , CM000675.1:g.24436369C>T	GRCh37
NC_000013.9:g.23334369C>T	NCBI36
NG_052977.1:g.32219G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382172.4:c.1053+72G>A MANE Select	ENSP00000371607.3:n.1053+72G>A
ENST00000382172.3:c.1053+72G>A	ENSP00000371607.3:n.1053+72G>A
ENST00000494139.1:n.450+72G>A
NM_005932.3:c.1053+72G>A	NP_005923.2:n.1053+72G>A
XM_011535097.1:c.867+72G>A	XP_011533399.1:n.867+72G>A
XM_011535098.1:c.1053+72G>A	XP_011533400.1:n.1053+72G>A
XM_011535097.2:c.867+72G>A	XP_011533399.1:n.867+72G>A
XM_011535098.3:c.1053+72G>A	XP_011533400.1:n.1053+72G>A
NM_005932.4:c.1053+72G>A MANE Select	NP_005923.3:n.1053+72G>A