Canonical Allele Identifier: CA482935850

Gene: MIPEP

Linked Data

• dbSNP Id: rs1192825882
• gnomAD v2: 13-24436492-T-C
• gnomAD v4: 13-23862353-T-C
• MyVariant Identifiers: chr13:g.24436492T>C (hg19) ; chr13:g.23862353T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23862353T>C , CM000675.2:g.23862353T>C	GRCh38
NC_000013.10:g.24436492T>C , CM000675.1:g.24436492T>C	GRCh37
NC_000013.9:g.23334492T>C	NCBI36
NG_052977.1:g.32096A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382172.4:c.1002A>G MANE Select	ENSP00000371607.3:p.Lys334=
ENST00000382172.3:c.1002A>G	ENSP00000371607.3:p.Lys334=
ENST00000494139.1:n.399A>G
NM_005932.3:c.1002A>G	NP_005923.2:p.Lys334=
XM_011535097.1:c.816A>G	XP_011533399.1:p.Lys272=
XM_011535098.1:c.1002A>G	XP_011533400.1:p.Lys334=
XM_011535097.2:c.816A>G	XP_011533399.1:p.Lys272=
XM_011535098.3:c.1002A>G	XP_011533400.1:p.Lys334=
NM_005932.4:c.1002A>G MANE Select	NP_005923.3:p.Lys334=