Canonical Allele Identifier: CA365254448

Gene: REV3L MFSD4B

Linked Data

• MyVariant Identifiers: chr6:g.111628695G>C (hg19) ; chr6:g.111307492G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111307492G>C , CM000668.2:g.111307492G>C	GRCh38
NC_000006.11:g.111628695G>C , CM000668.1:g.111628695G>C	GRCh37
NC_000006.10:g.111735388G>C	NCBI36
NG_053000.1:g.181224C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368802.8:c.9121C>G (REV3L) MANE Select	ENSP00000357792.3:p.His3041Asp
ENST00000666581.2:n.277+29334G>C (MFSD4B)
ENST00000673245.1:n.273+11717G>C (MFSD4B)
ENST00000673446.1:n.179+39655G>C (MFSD4B)
ENST00000358835.7:c.9121C>G (REV3L)	ENSP00000351697.3:p.His3041Asp
ENST00000368802.7:c.9121C>G (REV3L)	ENSP00000357792.3:p.His3041Asp
ENST00000368805.5:c.9121C>G (REV3L)	ENSP00000357795.1:p.His3041Asp
ENST00000422377.5:c.*9105C>G (REV3L)	ENSP00000393184.1:n.*9105C>G
ENST00000434009.5:c.*9212C>G (REV3L)	ENSP00000391605.1:n.*9212C>G
ENST00000435970.5:c.8887C>G (REV3L)	ENSP00000402003.1:p.His2963Asp
ENST00000462119.5:n.1258C>G (REV3L)
NM_001286431.1:c.8887C>G (REV3L)	NP_001273360.1:p.His2963Asp
NM_001286432.1:c.8887C>G (REV3L)	NP_001273361.1:p.His2963Asp
NM_002912.4:c.9121C>G (REV3L)	NP_002903.3:p.His3041Asp
XM_006715543.2:c.9121C>G (REV3L)	XP_006715606.1:p.His3041Asp
XM_006715544.2:c.8887C>G (REV3L)	XP_006715607.1:p.His2963Asp
XM_011536028.1:c.9202C>G (REV3L)	XP_011534330.1:p.His3068Asp
XM_011536029.1:c.9199C>G (REV3L)	XP_011534331.1:p.His3067Asp
XM_011536030.1:c.9124C>G (REV3L)	XP_011534332.1:p.His3042Asp
XM_011536031.1:c.8968C>G (REV3L)	XP_011534333.1:p.His2990Asp
XM_011536032.1:c.8968C>G (REV3L)	XP_011534334.1:p.His2990Asp
XR_942871.1:n.2045+29334G>C
XM_011536028.2:c.9202C>G (REV3L)	XP_011534330.1:p.His3068Asp
XM_011536029.3:c.9199C>G (REV3L)	XP_011534331.1:p.His3067Asp
XM_011536030.3:c.9124C>G (REV3L)	XP_011534332.1:p.His3042Asp
XM_011536031.3:c.8968C>G (REV3L)	XP_011534333.1:p.His2990Asp
XM_011536032.2:c.8968C>G (REV3L)	XP_011534334.1:p.His2990Asp
XM_017011152.2:c.8965C>G (REV3L)	XP_016866641.1:p.His2989Asp
XM_017011153.1:c.8965C>G (REV3L)	XP_016866642.1:p.His2989Asp
XM_017011154.1:c.8965C>G (REV3L)	XP_016866643.1:p.His2989Asp
XR_001743550.2:n.9307C>G (REV3L)
XR_001743552.2:n.9229C>G (REV3L)
XR_001743553.2:n.9625C>G (REV3L)
XR_001743555.2:n.9547C>G (REV3L)
XR_001743556.2:n.9354C>G (REV3L)
XR_002956293.1:n.10565C>G (REV3L)
NM_001286431.2:c.8887C>G (REV3L)	NP_001273360.1:p.His2963Asp
NM_001372078.1:c.9121C>G (REV3L) MANE Select	NP_001359007.1:p.His3041Asp
NM_001286432.2:c.8887C>G (REV3L)	NP_001273361.1:p.His2963Asp
NM_002912.5:c.9121C>G (REV3L)	NP_002903.3:p.His3041Asp