Canonical Allele Identifier: CA451780667

Gene: REV3L MFSD4B

Linked Data

• MyVariant Identifiers: chr6:g.111628633A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111307430A>T , CM000668.2:g.111307430A>T	GRCh38
NC_000006.11:g.111628633A>T , CM000668.1:g.111628633A>T	GRCh37
NC_000006.10:g.111735326A>T	NCBI36
NG_053000.1:g.181286T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368802.8:c.9183T>A (REV3L) MANE Select	ENSP00000357792.3:p.Pro3061=
ENST00000666581.2:n.277+29272A>T (MFSD4B)
ENST00000673245.1:n.273+11655A>T (MFSD4B)
ENST00000673446.1:n.179+39593A>T (MFSD4B)
ENST00000358835.7:c.9183T>A (REV3L)	ENSP00000351697.3:p.Pro3061=
ENST00000368802.7:c.9183T>A (REV3L)	ENSP00000357792.3:p.Pro3061=
ENST00000368805.5:c.9183T>A (REV3L)	ENSP00000357795.1:p.Pro3061=
ENST00000422377.5:c.*9167T>A (REV3L)	ENSP00000393184.1:n.*9167T>A
ENST00000434009.5:c.*9274T>A (REV3L)	ENSP00000391605.1:n.*9274T>A
ENST00000435970.5:c.8949T>A (REV3L)	ENSP00000402003.1:p.Pro2983=
ENST00000462119.5:n.1320T>A (REV3L)
NM_001286431.1:c.8949T>A (REV3L)	NP_001273360.1:p.Pro2983=
NM_001286432.1:c.8949T>A (REV3L)	NP_001273361.1:p.Pro2983=
NM_002912.4:c.9183T>A (REV3L)	NP_002903.3:p.Pro3061=
XM_006715543.2:c.9183T>A (REV3L)	XP_006715606.1:p.Pro3061=
XM_006715544.2:c.8949T>A (REV3L)	XP_006715607.1:p.Pro2983=
XM_011536028.1:c.9264T>A (REV3L)	XP_011534330.1:p.Pro3088=
XM_011536029.1:c.9261T>A (REV3L)	XP_011534331.1:p.Pro3087=
XM_011536030.1:c.9186T>A (REV3L)	XP_011534332.1:p.Pro3062=
XM_011536031.1:c.9030T>A (REV3L)	XP_011534333.1:p.Pro3010=
XM_011536032.1:c.9030T>A (REV3L)	XP_011534334.1:p.Pro3010=
XR_942871.1:n.2045+29272A>T
XM_011536028.2:c.9264T>A (REV3L)	XP_011534330.1:p.Pro3088=
XM_011536029.3:c.9261T>A (REV3L)	XP_011534331.1:p.Pro3087=
XM_011536030.3:c.9186T>A (REV3L)	XP_011534332.1:p.Pro3062=
XM_011536031.3:c.9030T>A (REV3L)	XP_011534333.1:p.Pro3010=
XM_011536032.2:c.9030T>A (REV3L)	XP_011534334.1:p.Pro3010=
XM_017011152.2:c.9027T>A (REV3L)	XP_016866641.1:p.Pro3009=
XM_017011153.1:c.9027T>A (REV3L)	XP_016866642.1:p.Pro3009=
XM_017011154.1:c.9027T>A (REV3L)	XP_016866643.1:p.Pro3009=
XR_001743550.2:n.9369T>A (REV3L)
XR_001743552.2:n.9291T>A (REV3L)
XR_001743553.2:n.9687T>A (REV3L)
XR_001743555.2:n.9609T>A (REV3L)
XR_001743556.2:n.9416T>A (REV3L)
XR_002956293.1:n.10627T>A (REV3L)
NM_001286431.2:c.8949T>A (REV3L)	NP_001273360.1:p.Pro2983=
NM_001372078.1:c.9183T>A (REV3L) MANE Select	NP_001359007.1:p.Pro3061=
NM_001286432.2:c.8949T>A (REV3L)	NP_001273361.1:p.Pro2983=
NM_002912.5:c.9183T>A (REV3L)	NP_002903.3:p.Pro3061=