Canonical Allele Identifier: CA1654886143
Gene: REV3L HGNC NCBI
MFSD4B HGNC NCBI

Linked Data

dbSNP Id: rs1055654094

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111352518A>C , CM000668.2:g.111352518A>C GRCh38
NC_000006.11:g.111673721A>C , CM000668.1:g.111673721A>C GRCh37
NC_000006.10:g.111780414A>C NCBI36
NG_053000.1:g.136198T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000368802.8:c.7185-727T>G (REV3L) MANE Select ENSP00000357792.3:n.7185-727T>G
ENST00000666581.2:n.278-3265A>C (MFSD4B)
ENST00000673446.1:n.180-3265A>C (MFSD4B)
ENST00000358835.7:c.7185-727T>G (REV3L) ENSP00000351697.3:n.7185-727T>G
ENST00000368802.7:c.7185-727T>G (REV3L) ENSP00000357792.3:n.7185-727T>G
ENST00000368805.5:c.7185-727T>G (REV3L) ENSP00000357795.1:n.7185-727T>G
ENST00000413831.1:c.563-727T>G (REV3L) ENSP00000400600.1:n.563-727T>G
ENST00000422377.5:c.*7169-727T>G (REV3L) ENSP00000393184.1:n.*7169-727T>G
ENST00000434009.5:c.*7276-727T>G (REV3L) ENSP00000391605.1:n.*7276-727T>G
ENST00000435970.5:c.6951-727T>G (REV3L) ENSP00000402003.1:n.6951-727T>G
NM_001286431.1:c.6951-727T>G (REV3L) NP_001273360.1:n.6951-727T>G
NM_001286432.1:c.6951-727T>G (REV3L) NP_001273361.1:n.6951-727T>G
NM_002912.4:c.7185-727T>G (REV3L) NP_002903.3:n.7185-727T>G
XM_006715543.2:c.7185-727T>G (REV3L) XP_006715606.1:n.7185-727T>G
XM_006715544.2:c.6951-727T>G (REV3L) XP_006715607.1:n.6951-727T>G
XM_011536028.1:c.7266-727T>G (REV3L) XP_011534330.1:n.7266-727T>G
XM_011536029.1:c.7263-727T>G (REV3L) XP_011534331.1:n.7263-727T>G
XM_011536030.1:c.7188-727T>G (REV3L) XP_011534332.1:n.7188-727T>G
XM_011536031.1:c.7032-727T>G (REV3L) XP_011534333.1:n.7032-727T>G
XM_011536032.1:c.7032-727T>G (REV3L) XP_011534334.1:n.7032-727T>G
XM_011536033.1:c.7266-727T>G (REV3L) XP_011534335.1:n.7266-727T>G
XM_011536034.1:c.7266-727T>G (REV3L) XP_011534336.1:n.7266-727T>G
XM_011536035.1:c.7188-727T>G (REV3L) XP_011534337.1:n.7188-727T>G
XR_942545.1:n.7544-727T>G (REV3L)
XM_011536028.2:c.7266-727T>G (REV3L) XP_011534330.1:n.7266-727T>G
XM_011536029.3:c.7263-727T>G (REV3L) XP_011534331.1:n.7263-727T>G
XM_011536030.3:c.7188-727T>G (REV3L) XP_011534332.1:n.7188-727T>G
XM_011536031.3:c.7032-727T>G (REV3L) XP_011534333.1:n.7032-727T>G
XM_011536032.2:c.7032-727T>G (REV3L) XP_011534334.1:n.7032-727T>G
XM_017011152.2:c.7029-727T>G (REV3L) XP_016866641.1:n.7029-727T>G
XM_017011153.1:c.7029-727T>G (REV3L) XP_016866642.1:n.7029-727T>G
XM_017011154.1:c.7029-727T>G (REV3L) XP_016866643.1:n.7029-727T>G
XR_001743550.2:n.7562-727T>G (REV3L)
XR_001743552.2:n.7484-727T>G (REV3L)
XR_001743553.2:n.7562-727T>G (REV3L)
XR_001743554.2:n.7562-727T>G (REV3L)
XR_001743555.2:n.7484-727T>G (REV3L)
XR_001743556.2:n.7291-727T>G (REV3L)
XR_002956293.1:n.7291-727T>G (REV3L)
NM_001286431.2:c.6951-727T>G (REV3L) NP_001273360.1:n.6951-727T>G
NM_001372078.1:c.7185-727T>G (REV3L) MANE Select NP_001359007.1:n.7185-727T>G
NM_001286432.2:c.6951-727T>G (REV3L) NP_001273361.1:n.6951-727T>G
NM_002912.5:c.7185-727T>G (REV3L) NP_002903.3:n.7185-727T>G