Canonical Allele Identifier: CA16620985
Gene: MRAP HGNC NCBI
MRAP-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 423392
ClinVar RCV Id: RCV000482985
dbSNP Id: rs1064796398

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.32306744G>T , CM000683.2:g.32306744G>T GRCh38
NC_000021.8:g.33679055G>T , CM000683.1:g.33679055G>T GRCh37
NC_000021.7:g.32600926G>T NCBI36
NG_016234.1:g.19932G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000303645.10:c.206+5G>T (MRAP) MANE Select ENSP00000306697.5:n.206+5G>T
ENST00000303645.9:c.206+5G>T (MRAP) ENSP00000306697.5:n.206+5G>T
ENST00000339944.4:c.206+5G>T (MRAP) ENSP00000343661.4:n.206+5G>T
ENST00000399784.6:c.206+5G>T (MRAP) ENSP00000382684.2:n.206+5G>T
ENST00000497833.1:n.277+5G>T (MRAP)
NM_001285394.1:c.29+5G>T (MRAP) NP_001272323.1:n.29+5G>T
NM_178817.3:c.206+5G>T (MRAP) NP_848932.1:n.206+5G>T
NM_206898.1:c.206+5G>T (MRAP) NP_996781.1:n.206+5G>T
XM_006724028.2:c.206+5G>T (MRAP) XP_006724091.1:n.206+5G>T
XR_937664.1:n.719C>A (MRAP-AS1)
XM_006724028.3:c.206+5G>T (MRAP) XP_006724091.1:n.206+5G>T
XM_017028407.1:c.206+5G>T (MRAP) XP_016883896.1:n.206+5G>T
NM_001285394.2:c.29+5G>T (MRAP) NP_001272323.1:n.29+5G>T
NM_178817.4:c.206+5G>T (MRAP) NP_848932.1:n.206+5G>T
NM_001379228.1:c.206+5G>T (MRAP) MANE Select NP_001366157.1:n.206+5G>T
NM_206898.2:c.206+5G>T (MRAP) NP_996781.1:n.206+5G>T