Canonical Allele Identifier: CA954128490

Gene: MIPEP

Linked Data

• dbSNP Id: rs1870339386
• gnomAD v3: 13-23862238-A-C
• gnomAD v4: 13-23862238-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23862238A>C , CM000675.2:g.23862238A>C	GRCh38
NC_000013.10:g.24436377A>C , CM000675.1:g.24436377A>C	GRCh37
NC_000013.9:g.23334377A>C	NCBI36
NG_052977.1:g.32211T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382172.4:c.1053+64T>G MANE Select	ENSP00000371607.3:n.1053+64T>G
ENST00000382172.3:c.1053+64T>G	ENSP00000371607.3:n.1053+64T>G
ENST00000494139.1:n.450+64T>G
NM_005932.3:c.1053+64T>G	NP_005923.2:n.1053+64T>G
XM_011535097.1:c.867+64T>G	XP_011533399.1:n.867+64T>G
XM_011535098.1:c.1053+64T>G	XP_011533400.1:n.1053+64T>G
XM_011535097.2:c.867+64T>G	XP_011533399.1:n.867+64T>G
XM_011535098.3:c.1053+64T>G	XP_011533400.1:n.1053+64T>G
NM_005932.4:c.1053+64T>G MANE Select	NP_005923.3:n.1053+64T>G