Canonical Allele Identifier: CA2360473426
Gene: MAPRE1 HGNC NCBI

Linked Data

dbSNP Id: rs187178

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32822473A>T , CM000682.2:g.32822473A>T GRCh38
NC_000020.10:g.31410279A>T , CM000682.1:g.31410279A>T GRCh37
NC_000020.9:g.30873940A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375571.6:c.-4+2445A>T MANE Select ENSP00000364721.5:n.-4+2445A>T
ENST00000375571.5:c.-4+2445A>T ENSP00000364721.5:n.-4+2445A>T
NM_012325.2:c.-4+2445A>T NP_036457.1:n.-4+2445A>T
XM_011528696.1:c.-4+2556A>T XP_011526998.1:n.-4+2556A>T
XM_011528696.2:c.-4+2556A>T XP_011526998.1:n.-4+2556A>T
NM_012325.3:c.-4+2445A>T MANE Select NP_036457.1:n.-4+2445A>T