Canonical Allele Identifier: CA365254608

Gene: REV3L MFSD4B

Linked Data

• MyVariant Identifiers: chr6:g.111628770G>C (hg19) ; chr6:g.111307567G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111307567G>C , CM000668.2:g.111307567G>C	GRCh38
NC_000006.11:g.111628770G>C , CM000668.1:g.111628770G>C	GRCh37
NC_000006.10:g.111735463G>C	NCBI36
NG_053000.1:g.181149C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368802.8:c.9046C>G (REV3L) MANE Select	ENSP00000357792.3:p.His3016Asp
ENST00000666581.2:n.277+29409G>C (MFSD4B)
ENST00000673245.1:n.273+11792G>C (MFSD4B)
ENST00000673446.1:n.179+39730G>C (MFSD4B)
ENST00000358835.7:c.9046C>G (REV3L)	ENSP00000351697.3:p.His3016Asp
ENST00000368802.7:c.9046C>G (REV3L)	ENSP00000357792.3:p.His3016Asp
ENST00000368805.5:c.9046C>G (REV3L)	ENSP00000357795.1:p.His3016Asp
ENST00000422377.5:c.*9030C>G (REV3L)	ENSP00000393184.1:n.*9030C>G
ENST00000434009.5:c.*9137C>G (REV3L)	ENSP00000391605.1:n.*9137C>G
ENST00000435970.5:c.8812C>G (REV3L)	ENSP00000402003.1:p.His2938Asp
ENST00000462119.5:n.1183C>G (REV3L)
NM_001286431.1:c.8812C>G (REV3L)	NP_001273360.1:p.His2938Asp
NM_001286432.1:c.8812C>G (REV3L)	NP_001273361.1:p.His2938Asp
NM_002912.4:c.9046C>G (REV3L)	NP_002903.3:p.His3016Asp
XM_006715543.2:c.9046C>G (REV3L)	XP_006715606.1:p.His3016Asp
XM_006715544.2:c.8812C>G (REV3L)	XP_006715607.1:p.His2938Asp
XM_011536028.1:c.9127C>G (REV3L)	XP_011534330.1:p.His3043Asp
XM_011536029.1:c.9124C>G (REV3L)	XP_011534331.1:p.His3042Asp
XM_011536030.1:c.9049C>G (REV3L)	XP_011534332.1:p.His3017Asp
XM_011536031.1:c.8893C>G (REV3L)	XP_011534333.1:p.His2965Asp
XM_011536032.1:c.8893C>G (REV3L)	XP_011534334.1:p.His2965Asp
XR_942871.1:n.2045+29409G>C
XM_011536028.2:c.9127C>G (REV3L)	XP_011534330.1:p.His3043Asp
XM_011536029.3:c.9124C>G (REV3L)	XP_011534331.1:p.His3042Asp
XM_011536030.3:c.9049C>G (REV3L)	XP_011534332.1:p.His3017Asp
XM_011536031.3:c.8893C>G (REV3L)	XP_011534333.1:p.His2965Asp
XM_011536032.2:c.8893C>G (REV3L)	XP_011534334.1:p.His2965Asp
XM_017011152.2:c.8890C>G (REV3L)	XP_016866641.1:p.His2964Asp
XM_017011153.1:c.8890C>G (REV3L)	XP_016866642.1:p.His2964Asp
XM_017011154.1:c.8890C>G (REV3L)	XP_016866643.1:p.His2964Asp
XR_001743550.2:n.9232C>G (REV3L)
XR_001743552.2:n.9154C>G (REV3L)
XR_001743553.2:n.9550C>G (REV3L)
XR_001743555.2:n.9472C>G (REV3L)
XR_001743556.2:n.9279C>G (REV3L)
XR_002956293.1:n.10490C>G (REV3L)
NM_001286431.2:c.8812C>G (REV3L)	NP_001273360.1:p.His2938Asp
NM_001372078.1:c.9046C>G (REV3L) MANE Select	NP_001359007.1:p.His3016Asp
NM_001286432.2:c.8812C>G (REV3L)	NP_001273361.1:p.His2938Asp
NM_002912.5:c.9046C>G (REV3L)	NP_002903.3:p.His3016Asp