Canonical Allele Identifier: CA608642653

Gene: MIPEP

Linked Data

• dbSNP Id: rs1260365172
• gnomAD v2: 13-24436399-C-A
• gnomAD v3: 13-23862260-C-A
• gnomAD v4: 13-23862260-C-A
• MyVariant Identifiers: chr13:g.24436399C>A (hg19) ; chr13:g.23862260C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23862260C>A , CM000675.2:g.23862260C>A	GRCh38
NC_000013.10:g.24436399C>A , CM000675.1:g.24436399C>A	GRCh37
NC_000013.9:g.23334399C>A	NCBI36
NG_052977.1:g.32189G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382172.4:c.1053+42G>T MANE Select	ENSP00000371607.3:n.1053+42G>T
ENST00000382172.3:c.1053+42G>T	ENSP00000371607.3:n.1053+42G>T
ENST00000494139.1:n.450+42G>T
NM_005932.3:c.1053+42G>T	NP_005923.2:n.1053+42G>T
XM_011535097.1:c.867+42G>T	XP_011533399.1:n.867+42G>T
XM_011535098.1:c.1053+42G>T	XP_011533400.1:n.1053+42G>T
XM_011535097.2:c.867+42G>T	XP_011533399.1:n.867+42G>T
XM_011535098.3:c.1053+42G>T	XP_011533400.1:n.1053+42G>T
NM_005932.4:c.1053+42G>T MANE Select	NP_005923.3:n.1053+42G>T