Canonical Allele Identifier: CA2622340314

Gene: MIPEP

Linked Data

• gnomAD v4: 13-23862263-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23862263A>C , CM000675.2:g.23862263A>C	GRCh38
NC_000013.10:g.24436402A>C , CM000675.1:g.24436402A>C	GRCh37
NC_000013.9:g.23334402A>C	NCBI36
NG_052977.1:g.32186T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382172.4:c.1053+39T>G MANE Select	ENSP00000371607.3:n.1053+39T>G
ENST00000382172.3:c.1053+39T>G	ENSP00000371607.3:n.1053+39T>G
ENST00000494139.1:n.450+39T>G
NM_005932.3:c.1053+39T>G	NP_005923.2:n.1053+39T>G
XM_011535097.1:c.867+39T>G	XP_011533399.1:n.867+39T>G
XM_011535098.1:c.1053+39T>G	XP_011533400.1:n.1053+39T>G
XM_011535097.2:c.867+39T>G	XP_011533399.1:n.867+39T>G
XM_011535098.3:c.1053+39T>G	XP_011533400.1:n.1053+39T>G
NM_005932.4:c.1053+39T>G MANE Select	NP_005923.3:n.1053+39T>G