Canonical Allele Identifier: CA2360473481
Gene: MAPRE1 HGNC NCBI

Linked Data

dbSNP Id: rs1982732919

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32822594A>C , CM000682.2:g.32822594A>C GRCh38
NC_000020.10:g.31410400A>C , CM000682.1:g.31410400A>C GRCh37
NC_000020.9:g.30874061A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375571.6:c.-4+2566A>C MANE Select ENSP00000364721.5:n.-4+2566A>C
ENST00000375571.5:c.-4+2566A>C ENSP00000364721.5:n.-4+2566A>C
NM_012325.2:c.-4+2566A>C NP_036457.1:n.-4+2566A>C
XM_011528696.1:c.-4+2677A>C XP_011526998.1:n.-4+2677A>C
XM_011528696.2:c.-4+2677A>C XP_011526998.1:n.-4+2677A>C
NM_012325.3:c.-4+2566A>C MANE Select NP_036457.1:n.-4+2566A>C