Canonical Allele Identifier: CA2772616376

Gene: REV3L MFSD4B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111352704_111352714del , CM000668.2:g.111352704_111352714del	GRCh38
NC_000006.11:g.111673907_111673917del , CM000668.1:g.111673907_111673917del	GRCh37
NC_000006.10:g.111780600_111780610del	NCBI36
NG_053000.1:g.136005_136015del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368802.8:c.7185-920_7185-910del (REV3L) MANE Select	ENSP00000357792.3:n.7185-920_7185-910del
ENST00000666581.2:n.278-3079_278-3069del (MFSD4B)
ENST00000673446.1:n.180-3079_180-3069del (MFSD4B)
ENST00000358835.7:c.7185-920_7185-910del (REV3L)	ENSP00000351697.3:n.7185-920_7185-910del
ENST00000368802.7:c.7185-920_7185-910del (REV3L)	ENSP00000357792.3:n.7185-920_7185-910del
ENST00000368805.5:c.7185-920_7185-910del (REV3L)	ENSP00000357795.1:n.7185-920_7185-910del
ENST00000413831.1:c.563-920_563-910del (REV3L)	ENSP00000400600.1:n.563-920_563-910del
ENST00000422377.5:c.*7169-920_*7169-910del (REV3L)	ENSP00000393184.1:n.*7169-920_*7169-910del
ENST00000434009.5:c.*7276-920_*7276-910del (REV3L)	ENSP00000391605.1:n.*7276-920_*7276-910del
ENST00000435970.5:c.6951-920_6951-910del (REV3L)	ENSP00000402003.1:n.6951-920_6951-910del
NM_001286431.1:c.6951-920_6951-910del (REV3L)	NP_001273360.1:n.6951-920_6951-910del
NM_001286432.1:c.6951-920_6951-910del (REV3L)	NP_001273361.1:n.6951-920_6951-910del
NM_002912.4:c.7185-920_7185-910del (REV3L)	NP_002903.3:n.7185-920_7185-910del
XM_006715543.2:c.7185-920_7185-910del (REV3L)	XP_006715606.1:n.7185-920_7185-910del
XM_006715544.2:c.6951-920_6951-910del (REV3L)	XP_006715607.1:n.6951-920_6951-910del
XM_011536028.1:c.7266-920_7266-910del (REV3L)	XP_011534330.1:n.7266-920_7266-910del
XM_011536029.1:c.7263-920_7263-910del (REV3L)	XP_011534331.1:n.7263-920_7263-910del
XM_011536030.1:c.7188-920_7188-910del (REV3L)	XP_011534332.1:n.7188-920_7188-910del
XM_011536031.1:c.7032-920_7032-910del (REV3L)	XP_011534333.1:n.7032-920_7032-910del
XM_011536032.1:c.7032-920_7032-910del (REV3L)	XP_011534334.1:n.7032-920_7032-910del
XM_011536033.1:c.7266-920_7266-910del (REV3L)	XP_011534335.1:n.7266-920_7266-910del
XM_011536034.1:c.7266-920_7266-910del (REV3L)	XP_011534336.1:n.7266-920_7266-910del
XM_011536035.1:c.7188-920_7188-910del (REV3L)	XP_011534337.1:n.7188-920_7188-910del
XR_942545.1:n.7544-920_7544-910del (REV3L)
XM_011536028.2:c.7266-920_7266-910del (REV3L)	XP_011534330.1:n.7266-920_7266-910del
XM_011536029.3:c.7263-920_7263-910del (REV3L)	XP_011534331.1:n.7263-920_7263-910del
XM_011536030.3:c.7188-920_7188-910del (REV3L)	XP_011534332.1:n.7188-920_7188-910del
XM_011536031.3:c.7032-920_7032-910del (REV3L)	XP_011534333.1:n.7032-920_7032-910del
XM_011536032.2:c.7032-920_7032-910del (REV3L)	XP_011534334.1:n.7032-920_7032-910del
XM_017011152.2:c.7029-920_7029-910del (REV3L)	XP_016866641.1:n.7029-920_7029-910del
XM_017011153.1:c.7029-920_7029-910del (REV3L)	XP_016866642.1:n.7029-920_7029-910del
XM_017011154.1:c.7029-920_7029-910del (REV3L)	XP_016866643.1:n.7029-920_7029-910del
XR_001743550.2:n.7562-920_7562-910del (REV3L)
XR_001743552.2:n.7484-920_7484-910del (REV3L)
XR_001743553.2:n.7562-920_7562-910del (REV3L)
XR_001743554.2:n.7562-920_7562-910del (REV3L)
XR_001743555.2:n.7484-920_7484-910del (REV3L)
XR_001743556.2:n.7291-920_7291-910del (REV3L)
XR_002956293.1:n.7291-920_7291-910del (REV3L)
NM_001286431.2:c.6951-920_6951-910del (REV3L)	NP_001273360.1:n.6951-920_6951-910del
NM_001372078.1:c.7185-920_7185-910del (REV3L) MANE Select	NP_001359007.1:n.7185-920_7185-910del
NM_001286432.2:c.6951-920_6951-910del (REV3L)	NP_001273361.1:n.6951-920_6951-910del
NM_002912.5:c.7185-920_7185-910del (REV3L)	NP_002903.3:n.7185-920_7185-910del