Canonical Allele Identifier: CA365254419

Gene: REV3L MFSD4B

Linked Data

• MyVariant Identifiers: chr6:g.111628682C>T (hg19) ; chr6:g.111307479C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111307479C>T , CM000668.2:g.111307479C>T	GRCh38
NC_000006.11:g.111628682C>T , CM000668.1:g.111628682C>T	GRCh37
NC_000006.10:g.111735375C>T	NCBI36
NG_053000.1:g.181237G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368802.8:c.9134G>A (REV3L) MANE Select	ENSP00000357792.3:p.Cys3045Tyr
ENST00000666581.2:n.277+29321C>T (MFSD4B)
ENST00000673245.1:n.273+11704C>T (MFSD4B)
ENST00000673446.1:n.179+39642C>T (MFSD4B)
ENST00000358835.7:c.9134G>A (REV3L)	ENSP00000351697.3:p.Cys3045Tyr
ENST00000368802.7:c.9134G>A (REV3L)	ENSP00000357792.3:p.Cys3045Tyr
ENST00000368805.5:c.9134G>A (REV3L)	ENSP00000357795.1:p.Cys3045Tyr
ENST00000422377.5:c.*9118G>A (REV3L)	ENSP00000393184.1:n.*9118G>A
ENST00000434009.5:c.*9225G>A (REV3L)	ENSP00000391605.1:n.*9225G>A
ENST00000435970.5:c.8900G>A (REV3L)	ENSP00000402003.1:p.Cys2967Tyr
ENST00000462119.5:n.1271G>A (REV3L)
NM_001286431.1:c.8900G>A (REV3L)	NP_001273360.1:p.Cys2967Tyr
NM_001286432.1:c.8900G>A (REV3L)	NP_001273361.1:p.Cys2967Tyr
NM_002912.4:c.9134G>A (REV3L)	NP_002903.3:p.Cys3045Tyr
XM_006715543.2:c.9134G>A (REV3L)	XP_006715606.1:p.Cys3045Tyr
XM_006715544.2:c.8900G>A (REV3L)	XP_006715607.1:p.Cys2967Tyr
XM_011536028.1:c.9215G>A (REV3L)	XP_011534330.1:p.Cys3072Tyr
XM_011536029.1:c.9212G>A (REV3L)	XP_011534331.1:p.Cys3071Tyr
XM_011536030.1:c.9137G>A (REV3L)	XP_011534332.1:p.Cys3046Tyr
XM_011536031.1:c.8981G>A (REV3L)	XP_011534333.1:p.Cys2994Tyr
XM_011536032.1:c.8981G>A (REV3L)	XP_011534334.1:p.Cys2994Tyr
XR_942871.1:n.2045+29321C>T
XM_011536028.2:c.9215G>A (REV3L)	XP_011534330.1:p.Cys3072Tyr
XM_011536029.3:c.9212G>A (REV3L)	XP_011534331.1:p.Cys3071Tyr
XM_011536030.3:c.9137G>A (REV3L)	XP_011534332.1:p.Cys3046Tyr
XM_011536031.3:c.8981G>A (REV3L)	XP_011534333.1:p.Cys2994Tyr
XM_011536032.2:c.8981G>A (REV3L)	XP_011534334.1:p.Cys2994Tyr
XM_017011152.2:c.8978G>A (REV3L)	XP_016866641.1:p.Cys2993Tyr
XM_017011153.1:c.8978G>A (REV3L)	XP_016866642.1:p.Cys2993Tyr
XM_017011154.1:c.8978G>A (REV3L)	XP_016866643.1:p.Cys2993Tyr
XR_001743550.2:n.9320G>A (REV3L)
XR_001743552.2:n.9242G>A (REV3L)
XR_001743553.2:n.9638G>A (REV3L)
XR_001743555.2:n.9560G>A (REV3L)
XR_001743556.2:n.9367G>A (REV3L)
XR_002956293.1:n.10578G>A (REV3L)
NM_001286431.2:c.8900G>A (REV3L)	NP_001273360.1:p.Cys2967Tyr
NM_001372078.1:c.9134G>A (REV3L) MANE Select	NP_001359007.1:p.Cys3045Tyr
NM_001286432.2:c.8900G>A (REV3L)	NP_001273361.1:p.Cys2967Tyr
NM_002912.5:c.9134G>A (REV3L)	NP_002903.3:p.Cys3045Tyr