Canonical Allele Identifier: CA145279980

Gene: REV3L MFSD4B

Linked Data

• dbSNP Id: rs985916889
• gnomAD v3: 6-111352411-ATGAG-A
• gnomAD v4: 6-111352411-ATGAG-A
• MyVariant Identifiers: chr6:g.111673615_111673618del (hg19) ; chr6:g.111352412_111352415del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111352415_111352418del , CM000668.2:g.111352415_111352418del	GRCh38
NC_000006.11:g.111673618_111673621del , CM000668.1:g.111673618_111673621del	GRCh37
NC_000006.10:g.111780311_111780314del	NCBI36
NG_053000.1:g.136301_136304del

Transcript Alleles

HGVS	Amino-acid change
ENST00000368802.8:c.7185-624_7185-621del (REV3L) MANE Select	ENSP00000357792.3:n.7185-624_7185-621del
ENST00000666581.2:n.278-3368_278-3365del (MFSD4B)
ENST00000673446.1:n.180-3368_180-3365del (MFSD4B)
ENST00000358835.7:c.7185-624_7185-621del (REV3L)	ENSP00000351697.3:n.7185-624_7185-621del
ENST00000368802.7:c.7185-624_7185-621del (REV3L)	ENSP00000357792.3:n.7185-624_7185-621del
ENST00000368805.5:c.7185-624_7185-621del (REV3L)	ENSP00000357795.1:n.7185-624_7185-621del
ENST00000413831.1:c.563-624_563-621del (REV3L)	ENSP00000400600.1:n.563-624_563-621del
ENST00000422377.5:c.*7169-624_*7169-621del (REV3L)	ENSP00000393184.1:n.*7169-624_*7169-621del
ENST00000434009.5:c.*7276-624_*7276-621del (REV3L)	ENSP00000391605.1:n.*7276-624_*7276-621del
ENST00000435970.5:c.6951-624_6951-621del (REV3L)	ENSP00000402003.1:n.6951-624_6951-621del
NM_001286431.1:c.6951-624_6951-621del (REV3L)	NP_001273360.1:n.6951-624_6951-621del
NM_001286432.1:c.6951-624_6951-621del (REV3L)	NP_001273361.1:n.6951-624_6951-621del
NM_002912.4:c.7185-624_7185-621del (REV3L)	NP_002903.3:n.7185-624_7185-621del
XM_006715543.2:c.7185-624_7185-621del (REV3L)	XP_006715606.1:n.7185-624_7185-621del
XM_006715544.2:c.6951-624_6951-621del (REV3L)	XP_006715607.1:n.6951-624_6951-621del
XM_011536028.1:c.7266-624_7266-621del (REV3L)	XP_011534330.1:n.7266-624_7266-621del
XM_011536029.1:c.7263-624_7263-621del (REV3L)	XP_011534331.1:n.7263-624_7263-621del
XM_011536030.1:c.7188-624_7188-621del (REV3L)	XP_011534332.1:n.7188-624_7188-621del
XM_011536031.1:c.7032-624_7032-621del (REV3L)	XP_011534333.1:n.7032-624_7032-621del
XM_011536032.1:c.7032-624_7032-621del (REV3L)	XP_011534334.1:n.7032-624_7032-621del
XM_011536033.1:c.7266-624_7266-621del (REV3L)	XP_011534335.1:n.7266-624_7266-621del
XM_011536034.1:c.7266-624_7266-621del (REV3L)	XP_011534336.1:n.7266-624_7266-621del
XM_011536035.1:c.7188-624_7188-621del (REV3L)	XP_011534337.1:n.7188-624_7188-621del
XR_942545.1:n.7544-624_7544-621del (REV3L)
XM_011536028.2:c.7266-624_7266-621del (REV3L)	XP_011534330.1:n.7266-624_7266-621del
XM_011536029.3:c.7263-624_7263-621del (REV3L)	XP_011534331.1:n.7263-624_7263-621del
XM_011536030.3:c.7188-624_7188-621del (REV3L)	XP_011534332.1:n.7188-624_7188-621del
XM_011536031.3:c.7032-624_7032-621del (REV3L)	XP_011534333.1:n.7032-624_7032-621del
XM_011536032.2:c.7032-624_7032-621del (REV3L)	XP_011534334.1:n.7032-624_7032-621del
XM_017011152.2:c.7029-624_7029-621del (REV3L)	XP_016866641.1:n.7029-624_7029-621del
XM_017011153.1:c.7029-624_7029-621del (REV3L)	XP_016866642.1:n.7029-624_7029-621del
XM_017011154.1:c.7029-624_7029-621del (REV3L)	XP_016866643.1:n.7029-624_7029-621del
XR_001743550.2:n.7562-624_7562-621del (REV3L)
XR_001743552.2:n.7484-624_7484-621del (REV3L)
XR_001743553.2:n.7562-624_7562-621del (REV3L)
XR_001743554.2:n.7562-624_7562-621del (REV3L)
XR_001743555.2:n.7484-624_7484-621del (REV3L)
XR_001743556.2:n.7291-624_7291-621del (REV3L)
XR_002956293.1:n.7291-624_7291-621del (REV3L)
NM_001286431.2:c.6951-624_6951-621del (REV3L)	NP_001273360.1:n.6951-624_6951-621del
NM_001372078.1:c.7185-624_7185-621del (REV3L) MANE Select	NP_001359007.1:n.7185-624_7185-621del
NM_001286432.2:c.6951-624_6951-621del (REV3L)	NP_001273361.1:n.6951-624_6951-621del
NM_002912.5:c.7185-624_7185-621del (REV3L)	NP_002903.3:n.7185-624_7185-621del