Canonical Allele Identifier: CA1654866901

Gene: REV3L MFSD4B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111307485G= , CM000668.2:g.111307485G=	GRCh38
NC_000006.11:g.111628688G= , CM000668.1:g.111628688G=	GRCh37
NC_000006.10:g.111735381G=	NCBI36
NG_053000.1:g.181231C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368802.8:c.9128C= (REV3L) MANE Select	ENSP00000357792.3:p.Pro3043=
ENST00000666581.2:n.277+29327G= (MFSD4B)
ENST00000673245.1:n.273+11710G= (MFSD4B)
ENST00000673446.1:n.179+39648G= (MFSD4B)
ENST00000358835.7:c.9128C= (REV3L)	ENSP00000351697.3:p.Pro3043=
ENST00000368802.7:c.9128C= (REV3L)	ENSP00000357792.3:p.Pro3043=
ENST00000368805.5:c.9128C= (REV3L)	ENSP00000357795.1:p.Pro3043=
ENST00000422377.5:c.*9112C= (REV3L)	ENSP00000393184.1:n.*9112C=
ENST00000434009.5:c.*9219C= (REV3L)	ENSP00000391605.1:n.*9219C=
ENST00000435970.5:c.8894C= (REV3L)	ENSP00000402003.1:p.Pro2965=
ENST00000462119.5:n.1265C= (REV3L)
NM_001286431.1:c.8894C= (REV3L)	NP_001273360.1:p.Pro2965=
NM_001286432.1:c.8894C= (REV3L)	NP_001273361.1:p.Pro2965=
NM_002912.4:c.9128C= (REV3L)	NP_002903.3:p.Pro3043=
XM_006715543.2:c.9128C= (REV3L)	XP_006715606.1:p.Pro3043=
XM_006715544.2:c.8894C= (REV3L)	XP_006715607.1:p.Pro2965=
XM_011536028.1:c.9209C= (REV3L)	XP_011534330.1:p.Pro3070=
XM_011536029.1:c.9206C= (REV3L)	XP_011534331.1:p.Pro3069=
XM_011536030.1:c.9131C= (REV3L)	XP_011534332.1:p.Pro3044=
XM_011536031.1:c.8975C= (REV3L)	XP_011534333.1:p.Pro2992=
XM_011536032.1:c.8975C= (REV3L)	XP_011534334.1:p.Pro2992=
XR_942871.1:n.2045+29327G=
XM_011536028.2:c.9209C= (REV3L)	XP_011534330.1:p.Pro3070=
XM_011536029.3:c.9206C= (REV3L)	XP_011534331.1:p.Pro3069=
XM_011536030.3:c.9131C= (REV3L)	XP_011534332.1:p.Pro3044=
XM_011536031.3:c.8975C= (REV3L)	XP_011534333.1:p.Pro2992=
XM_011536032.2:c.8975C= (REV3L)	XP_011534334.1:p.Pro2992=
XM_017011152.2:c.8972C= (REV3L)	XP_016866641.1:p.Pro2991=
XM_017011153.1:c.8972C= (REV3L)	XP_016866642.1:p.Pro2991=
XM_017011154.1:c.8972C= (REV3L)	XP_016866643.1:p.Pro2991=
XR_001743550.2:n.9314C= (REV3L)
XR_001743552.2:n.9236C= (REV3L)
XR_001743553.2:n.9632C= (REV3L)
XR_001743555.2:n.9554C= (REV3L)
XR_001743556.2:n.9361C= (REV3L)
XR_002956293.1:n.10572C= (REV3L)
NM_001286431.2:c.8894C= (REV3L)	NP_001273360.1:p.Pro2965=
NM_001372078.1:c.9128C= (REV3L) MANE Select	NP_001359007.1:p.Pro3043=
NM_001286432.2:c.8894C= (REV3L)	NP_001273361.1:p.Pro2965=
NM_002912.5:c.9128C= (REV3L)	NP_002903.3:p.Pro3043=