Canonical Allele Identifier: CA451780656

Gene: REV3L MFSD4B

Linked Data

• MyVariant Identifiers: chr6:g.111628618G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111307415G>T , CM000668.2:g.111307415G>T	GRCh38
NC_000006.11:g.111628618G>T , CM000668.1:g.111628618G>T	GRCh37
NC_000006.10:g.111735311G>T	NCBI36
NG_053000.1:g.181301C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368802.8:c.9198C>A (REV3L) MANE Select	ENSP00000357792.3:p.Val3066=
ENST00000666581.2:n.277+29257G>T (MFSD4B)
ENST00000673245.1:n.273+11640G>T (MFSD4B)
ENST00000673446.1:n.179+39578G>T (MFSD4B)
ENST00000358835.7:c.9198C>A (REV3L)	ENSP00000351697.3:p.Val3066=
ENST00000368802.7:c.9198C>A (REV3L)	ENSP00000357792.3:p.Val3066=
ENST00000368805.5:c.9198C>A (REV3L)	ENSP00000357795.1:p.Val3066=
ENST00000422377.5:c.*9182C>A (REV3L)	ENSP00000393184.1:n.*9182C>A
ENST00000434009.5:c.*9289C>A (REV3L)	ENSP00000391605.1:n.*9289C>A
ENST00000435970.5:c.8964C>A (REV3L)	ENSP00000402003.1:p.Val2988=
ENST00000462119.5:n.1335C>A (REV3L)
NM_001286431.1:c.8964C>A (REV3L)	NP_001273360.1:p.Val2988=
NM_001286432.1:c.8964C>A (REV3L)	NP_001273361.1:p.Val2988=
NM_002912.4:c.9198C>A (REV3L)	NP_002903.3:p.Val3066=
XM_006715543.2:c.9198C>A (REV3L)	XP_006715606.1:p.Val3066=
XM_006715544.2:c.8964C>A (REV3L)	XP_006715607.1:p.Val2988=
XM_011536028.1:c.9279C>A (REV3L)	XP_011534330.1:p.Val3093=
XM_011536029.1:c.9276C>A (REV3L)	XP_011534331.1:p.Val3092=
XM_011536030.1:c.9201C>A (REV3L)	XP_011534332.1:p.Val3067=
XM_011536031.1:c.9045C>A (REV3L)	XP_011534333.1:p.Val3015=
XM_011536032.1:c.9045C>A (REV3L)	XP_011534334.1:p.Val3015=
XR_942871.1:n.2045+29257G>T
XM_011536028.2:c.9279C>A (REV3L)	XP_011534330.1:p.Val3093=
XM_011536029.3:c.9276C>A (REV3L)	XP_011534331.1:p.Val3092=
XM_011536030.3:c.9201C>A (REV3L)	XP_011534332.1:p.Val3067=
XM_011536031.3:c.9045C>A (REV3L)	XP_011534333.1:p.Val3015=
XM_011536032.2:c.9045C>A (REV3L)	XP_011534334.1:p.Val3015=
XM_017011152.2:c.9042C>A (REV3L)	XP_016866641.1:p.Val3014=
XM_017011153.1:c.9042C>A (REV3L)	XP_016866642.1:p.Val3014=
XM_017011154.1:c.9042C>A (REV3L)	XP_016866643.1:p.Val3014=
XR_001743550.2:n.9384C>A (REV3L)
XR_001743552.2:n.9306C>A (REV3L)
XR_001743553.2:n.9702C>A (REV3L)
XR_001743555.2:n.9624C>A (REV3L)
XR_001743556.2:n.9431C>A (REV3L)
XR_002956293.1:n.10642C>A (REV3L)
NM_001286431.2:c.8964C>A (REV3L)	NP_001273360.1:p.Val2988=
NM_001372078.1:c.9198C>A (REV3L) MANE Select	NP_001359007.1:p.Val3066=
NM_001286432.2:c.8964C>A (REV3L)	NP_001273361.1:p.Val2988=
NM_002912.5:c.9198C>A (REV3L)	NP_002903.3:p.Val3066=