Canonical Allele Identifier: CA1654866981
Gene: REV3L HGNC NCBI
MFSD4B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111307665_111307669delinsATTCG , CM000668.2:g.111307665_111307669delinsATTCG GRCh38
NC_000006.11:g.111628868_111628872delinsATTCG , CM000668.1:g.111628868_111628872delinsATTCG GRCh37
NC_000006.10:g.111735561_111735565delinsATTCG NCBI36
NG_053000.1:g.181047_181051delinsCGAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368802.8:c.9043-99_9043-95delinsCGAAT (REV3L) MANE Select ENSP00000357792.3:n.9043-99_9043-95delinsCGAAT
ENST00000666581.2:n.277+29507_277+29511delinsATTCG (MFSD4B)
ENST00000673245.1:n.273+11890_273+11894delinsATTCG (MFSD4B)
ENST00000673446.1:n.179+39828_179+39832delinsATTCG (MFSD4B)
ENST00000358835.7:c.9043-99_9043-95delinsCGAAT (REV3L) ENSP00000351697.3:n.9043-99_9043-95delinsCGAAT
ENST00000368802.7:c.9043-99_9043-95delinsCGAAT (REV3L) ENSP00000357792.3:n.9043-99_9043-95delinsCGAAT
ENST00000368805.5:c.9043-99_9043-95delinsCGAAT (REV3L) ENSP00000357795.1:n.9043-99_9043-95delinsCGAAT
ENST00000422377.5:c.*9027-99_*9027-95delinsCGAAT (REV3L) ENSP00000393184.1:n.*9027-99_*9027-95delinsCGAAT
ENST00000434009.5:c.*9134-99_*9134-95delinsCGAAT (REV3L) ENSP00000391605.1:n.*9134-99_*9134-95delinsCGAAT
ENST00000435970.5:c.8809-99_8809-95delinsCGAAT (REV3L) ENSP00000402003.1:n.8809-99_8809-95delinsCGAAT
ENST00000462119.5:n.1180-99_1180-95delinsCGAAT (REV3L)
NM_001286431.1:c.8809-99_8809-95delinsCGAAT (REV3L) NP_001273360.1:n.8809-99_8809-95delinsCGAAT
NM_001286432.1:c.8809-99_8809-95delinsCGAAT (REV3L) NP_001273361.1:n.8809-99_8809-95delinsCGAAT
NM_002912.4:c.9043-99_9043-95delinsCGAAT (REV3L) NP_002903.3:n.9043-99_9043-95delinsCGAAT
XM_006715543.2:c.9043-99_9043-95delinsCGAAT (REV3L) XP_006715606.1:n.9043-99_9043-95delinsCGAAT
XM_006715544.2:c.8809-99_8809-95delinsCGAAT (REV3L) XP_006715607.1:n.8809-99_8809-95delinsCGAAT
XM_011536028.1:c.9124-99_9124-95delinsCGAAT (REV3L) XP_011534330.1:n.9124-99_9124-95delinsCGAAT
XM_011536029.1:c.9121-99_9121-95delinsCGAAT (REV3L) XP_011534331.1:n.9121-99_9121-95delinsCGAAT
XM_011536030.1:c.9046-99_9046-95delinsCGAAT (REV3L) XP_011534332.1:n.9046-99_9046-95delinsCGAAT
XM_011536031.1:c.8890-99_8890-95delinsCGAAT (REV3L) XP_011534333.1:n.8890-99_8890-95delinsCGAAT
XM_011536032.1:c.8890-99_8890-95delinsCGAAT (REV3L) XP_011534334.1:n.8890-99_8890-95delinsCGAAT
XR_942871.1:n.2045+29507_2045+29511delinsATTCG
XM_011536028.2:c.9124-99_9124-95delinsCGAAT (REV3L) XP_011534330.1:n.9124-99_9124-95delinsCGAAT
XM_011536029.3:c.9121-99_9121-95delinsCGAAT (REV3L) XP_011534331.1:n.9121-99_9121-95delinsCGAAT
XM_011536030.3:c.9046-99_9046-95delinsCGAAT (REV3L) XP_011534332.1:n.9046-99_9046-95delinsCGAAT
XM_011536031.3:c.8890-99_8890-95delinsCGAAT (REV3L) XP_011534333.1:n.8890-99_8890-95delinsCGAAT
XM_011536032.2:c.8890-99_8890-95delinsCGAAT (REV3L) XP_011534334.1:n.8890-99_8890-95delinsCGAAT
XM_017011152.2:c.8887-99_8887-95delinsCGAAT (REV3L) XP_016866641.1:n.8887-99_8887-95delinsCGAAT
XM_017011153.1:c.8887-99_8887-95delinsCGAAT (REV3L) XP_016866642.1:n.8887-99_8887-95delinsCGAAT
XM_017011154.1:c.8887-99_8887-95delinsCGAAT (REV3L) XP_016866643.1:n.8887-99_8887-95delinsCGAAT
XR_001743550.2:n.9229-99_9229-95delinsCGAAT (REV3L)
XR_001743552.2:n.9151-99_9151-95delinsCGAAT (REV3L)
XR_001743553.2:n.9547-99_9547-95delinsCGAAT (REV3L)
XR_001743555.2:n.9469-99_9469-95delinsCGAAT (REV3L)
XR_001743556.2:n.9276-99_9276-95delinsCGAAT (REV3L)
XR_002956293.1:n.10487-99_10487-95delinsCGAAT (REV3L)
NM_001286431.2:c.8809-99_8809-95delinsCGAAT (REV3L) NP_001273360.1:n.8809-99_8809-95delinsCGAAT
NM_001372078.1:c.9043-99_9043-95delinsCGAAT (REV3L) MANE Select NP_001359007.1:n.9043-99_9043-95delinsCGAAT
NM_001286432.2:c.8809-99_8809-95delinsCGAAT (REV3L) NP_001273361.1:n.8809-99_8809-95delinsCGAAT
NM_002912.5:c.9043-99_9043-95delinsCGAAT (REV3L) NP_002903.3:n.9043-99_9043-95delinsCGAAT