Canonical Allele Identifier: CA2654238636

Gene: MRAP

Linked Data

• gnomAD v4: 21-32299105-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.32299105G>T , CM000683.2:g.32299105G>T	GRCh38
NC_000021.8:g.33671416G>T , CM000683.1:g.33671416G>T	GRCh37
NC_000021.7:g.32593287G>T	NCBI36
NG_016234.1:g.12293G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303645.10:c.106+28G>T MANE Select	ENSP00000306697.5:n.106+28G>T
ENST00000303645.9:c.106+28G>T	ENSP00000306697.5:n.106+28G>T
ENST00000339944.4:c.106+28G>T	ENSP00000343661.4:n.106+28G>T
ENST00000399784.6:c.106+28G>T	ENSP00000382684.2:n.106+28G>T
ENST00000497833.1:n.177+5973G>T
NM_001285394.1:c.-72+5973G>T	NP_001272323.1:n.-72+5973G>T
NM_178817.3:c.106+28G>T	NP_848932.1:n.106+28G>T
NM_206898.1:c.106+28G>T	NP_996781.1:n.106+28G>T
XM_006724028.2:c.106+28G>T	XP_006724091.1:n.106+28G>T
XM_006724028.3:c.106+28G>T	XP_006724091.1:n.106+28G>T
XM_017028407.1:c.106+28G>T	XP_016883896.1:n.106+28G>T
NM_001285394.2:c.-72+5973G>T	NP_001272323.1:n.-72+5973G>T
NM_178817.4:c.106+28G>T	NP_848932.1:n.106+28G>T
NM_001379228.1:c.106+28G>T MANE Select	NP_001366157.1:n.106+28G>T
NM_206898.2:c.106+28G>T	NP_996781.1:n.106+28G>T