Canonical Allele Identifier: CA2360473467
Gene: MAPRE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32822554A= , CM000682.2:g.32822554A= GRCh38
NC_000020.10:g.31410360A= , CM000682.1:g.31410360A= GRCh37
NC_000020.9:g.30874021A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375571.6:c.-4+2526A= MANE Select ENSP00000364721.5:n.-4+2526A=
ENST00000375571.5:c.-4+2526A= ENSP00000364721.5:n.-4+2526A=
NM_012325.2:c.-4+2526A= NP_036457.1:n.-4+2526A=
XM_011528696.1:c.-4+2637A= XP_011526998.1:n.-4+2637A=
XM_011528696.2:c.-4+2637A= XP_011526998.1:n.-4+2637A=
NM_012325.3:c.-4+2526A= MANE Select NP_036457.1:n.-4+2526A=