Canonical Allele Identifier: CA451780699

Gene: REV3L MFSD4B

Linked Data

• MyVariant Identifiers: chr6:g.111628698A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111307495A>G , CM000668.2:g.111307495A>G	GRCh38
NC_000006.11:g.111628698A>G , CM000668.1:g.111628698A>G	GRCh37
NC_000006.10:g.111735391A>G	NCBI36
NG_053000.1:g.181221T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368802.8:c.9118T>C (REV3L) MANE Select	ENSP00000357792.3:p.Leu3040=
ENST00000666581.2:n.277+29337A>G (MFSD4B)
ENST00000673245.1:n.273+11720A>G (MFSD4B)
ENST00000673446.1:n.179+39658A>G (MFSD4B)
ENST00000358835.7:c.9118T>C (REV3L)	ENSP00000351697.3:p.Leu3040=
ENST00000368802.7:c.9118T>C (REV3L)	ENSP00000357792.3:p.Leu3040=
ENST00000368805.5:c.9118T>C (REV3L)	ENSP00000357795.1:p.Leu3040=
ENST00000422377.5:c.*9102T>C (REV3L)	ENSP00000393184.1:n.*9102T>C
ENST00000434009.5:c.*9209T>C (REV3L)	ENSP00000391605.1:n.*9209T>C
ENST00000435970.5:c.8884T>C (REV3L)	ENSP00000402003.1:p.Leu2962=
ENST00000462119.5:n.1255T>C (REV3L)
NM_001286431.1:c.8884T>C (REV3L)	NP_001273360.1:p.Leu2962=
NM_001286432.1:c.8884T>C (REV3L)	NP_001273361.1:p.Leu2962=
NM_002912.4:c.9118T>C (REV3L)	NP_002903.3:p.Leu3040=
XM_006715543.2:c.9118T>C (REV3L)	XP_006715606.1:p.Leu3040=
XM_006715544.2:c.8884T>C (REV3L)	XP_006715607.1:p.Leu2962=
XM_011536028.1:c.9199T>C (REV3L)	XP_011534330.1:p.Leu3067=
XM_011536029.1:c.9196T>C (REV3L)	XP_011534331.1:p.Leu3066=
XM_011536030.1:c.9121T>C (REV3L)	XP_011534332.1:p.Leu3041=
XM_011536031.1:c.8965T>C (REV3L)	XP_011534333.1:p.Leu2989=
XM_011536032.1:c.8965T>C (REV3L)	XP_011534334.1:p.Leu2989=
XR_942871.1:n.2045+29337A>G
XM_011536028.2:c.9199T>C (REV3L)	XP_011534330.1:p.Leu3067=
XM_011536029.3:c.9196T>C (REV3L)	XP_011534331.1:p.Leu3066=
XM_011536030.3:c.9121T>C (REV3L)	XP_011534332.1:p.Leu3041=
XM_011536031.3:c.8965T>C (REV3L)	XP_011534333.1:p.Leu2989=
XM_011536032.2:c.8965T>C (REV3L)	XP_011534334.1:p.Leu2989=
XM_017011152.2:c.8962T>C (REV3L)	XP_016866641.1:p.Leu2988=
XM_017011153.1:c.8962T>C (REV3L)	XP_016866642.1:p.Leu2988=
XM_017011154.1:c.8962T>C (REV3L)	XP_016866643.1:p.Leu2988=
XR_001743550.2:n.9304T>C (REV3L)
XR_001743552.2:n.9226T>C (REV3L)
XR_001743553.2:n.9622T>C (REV3L)
XR_001743555.2:n.9544T>C (REV3L)
XR_001743556.2:n.9351T>C (REV3L)
XR_002956293.1:n.10562T>C (REV3L)
NM_001286431.2:c.8884T>C (REV3L)	NP_001273360.1:p.Leu2962=
NM_001372078.1:c.9118T>C (REV3L) MANE Select	NP_001359007.1:p.Leu3040=
NM_001286432.2:c.8884T>C (REV3L)	NP_001273361.1:p.Leu2962=
NM_002912.5:c.9118T>C (REV3L)	NP_002903.3:p.Leu3040=