Canonical Allele Identifier: CA2654238673

Gene: MRAP

Linked Data

• gnomAD v4: 21-32299161-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.32299161T>A , CM000683.2:g.32299161T>A	GRCh38
NC_000021.8:g.33671472T>A , CM000683.1:g.33671472T>A	GRCh37
NC_000021.7:g.32593343T>A	NCBI36
NG_016234.1:g.12349T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303645.10:c.106+84T>A MANE Select	ENSP00000306697.5:n.106+84T>A
ENST00000303645.9:c.106+84T>A	ENSP00000306697.5:n.106+84T>A
ENST00000339944.4:c.106+84T>A	ENSP00000343661.4:n.106+84T>A
ENST00000399784.6:c.106+84T>A	ENSP00000382684.2:n.106+84T>A
ENST00000497833.1:n.177+6029T>A
NM_001285394.1:c.-72+6029T>A	NP_001272323.1:n.-72+6029T>A
NM_178817.3:c.106+84T>A	NP_848932.1:n.106+84T>A
NM_206898.1:c.106+84T>A	NP_996781.1:n.106+84T>A
XM_006724028.2:c.106+84T>A	XP_006724091.1:n.106+84T>A
XM_006724028.3:c.106+84T>A	XP_006724091.1:n.106+84T>A
XM_017028407.1:c.106+84T>A	XP_016883896.1:n.106+84T>A
NM_001285394.2:c.-72+6029T>A	NP_001272323.1:n.-72+6029T>A
NM_178817.4:c.106+84T>A	NP_848932.1:n.106+84T>A
NM_001379228.1:c.106+84T>A MANE Select	NP_001366157.1:n.106+84T>A
NM_206898.2:c.106+84T>A	NP_996781.1:n.106+84T>A