Canonical Allele Identifier: CA6913133

Gene: MIPEP

Linked Data

• dbSNP Id: rs778749647
• ExAC: 13:24436402 A / T
• gnomAD v2: 13-24436402-A-T
• gnomAD v4: 13-23862263-A-T
• MyVariant Identifiers: chr13:g.24436402A>T (hg19) ; chr13:g.23862263A>T (hg38)

Genomic Alleles

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

Transcript Alleles

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