Canonical Allele Identifier: CA145256953

Gene: REV3L MFSD4B

Linked Data

• dbSNP Id: rs369757323
• gnomAD v3: 6-111307570-T-C
• gnomAD v4: 6-111307570-T-C
• MyVariant Identifiers: chr6:g.111628773T>C (hg19) ; chr6:g.111307570T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111307570T>C , CM000668.2:g.111307570T>C	GRCh38
NC_000006.11:g.111628773T>C , CM000668.1:g.111628773T>C	GRCh37
NC_000006.10:g.111735466T>C	NCBI36
NG_053000.1:g.181146A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368802.8:c.9043A>G (REV3L) MANE Select	ENSP00000357792.3:p.Ile3015Val
ENST00000666581.2:n.277+29412T>C (MFSD4B)
ENST00000673245.1:n.273+11795T>C (MFSD4B)
ENST00000673446.1:n.179+39733T>C (MFSD4B)
ENST00000358835.7:c.9043A>G (REV3L)	ENSP00000351697.3:p.Ile3015Val
ENST00000368802.7:c.9043A>G (REV3L)	ENSP00000357792.3:p.Ile3015Val
ENST00000368805.5:c.9043A>G (REV3L)	ENSP00000357795.1:p.Ile3015Val
ENST00000422377.5:c.*9027A>G (REV3L)	ENSP00000393184.1:n.*9027A>G
ENST00000434009.5:c.*9134A>G (REV3L)	ENSP00000391605.1:n.*9134A>G
ENST00000435970.5:c.8809A>G (REV3L)	ENSP00000402003.1:p.Ile2937Val
ENST00000462119.5:n.1180A>G (REV3L)
NM_001286431.1:c.8809A>G (REV3L)	NP_001273360.1:p.Ile2937Val
NM_001286432.1:c.8809A>G (REV3L)	NP_001273361.1:p.Ile2937Val
NM_002912.4:c.9043A>G (REV3L)	NP_002903.3:p.Ile3015Val
XM_006715543.2:c.9043A>G (REV3L)	XP_006715606.1:p.Ile3015Val
XM_006715544.2:c.8809A>G (REV3L)	XP_006715607.1:p.Ile2937Val
XM_011536028.1:c.9124A>G (REV3L)	XP_011534330.1:p.Ile3042Val
XM_011536029.1:c.9121A>G (REV3L)	XP_011534331.1:p.Ile3041Val
XM_011536030.1:c.9046A>G (REV3L)	XP_011534332.1:p.Ile3016Val
XM_011536031.1:c.8890A>G (REV3L)	XP_011534333.1:p.Ile2964Val
XM_011536032.1:c.8890A>G (REV3L)	XP_011534334.1:p.Ile2964Val
XR_942871.1:n.2045+29412T>C
XM_011536028.2:c.9124A>G (REV3L)	XP_011534330.1:p.Ile3042Val
XM_011536029.3:c.9121A>G (REV3L)	XP_011534331.1:p.Ile3041Val
XM_011536030.3:c.9046A>G (REV3L)	XP_011534332.1:p.Ile3016Val
XM_011536031.3:c.8890A>G (REV3L)	XP_011534333.1:p.Ile2964Val
XM_011536032.2:c.8890A>G (REV3L)	XP_011534334.1:p.Ile2964Val
XM_017011152.2:c.8887A>G (REV3L)	XP_016866641.1:p.Ile2963Val
XM_017011153.1:c.8887A>G (REV3L)	XP_016866642.1:p.Ile2963Val
XM_017011154.1:c.8887A>G (REV3L)	XP_016866643.1:p.Ile2963Val
XR_001743550.2:n.9229A>G (REV3L)
XR_001743552.2:n.9151A>G (REV3L)
XR_001743553.2:n.9547A>G (REV3L)
XR_001743555.2:n.9469A>G (REV3L)
XR_001743556.2:n.9276A>G (REV3L)
XR_002956293.1:n.10487A>G (REV3L)
NM_001286431.2:c.8809A>G (REV3L)	NP_001273360.1:p.Ile2937Val
NM_001372078.1:c.9043A>G (REV3L) MANE Select	NP_001359007.1:p.Ile3015Val
NM_001286432.2:c.8809A>G (REV3L)	NP_001273361.1:p.Ile2937Val
NM_002912.5:c.9043A>G (REV3L)	NP_002903.3:p.Ile3015Val