Canonical Allele Identifier: CA2527363314

Gene: REV3L MFSD4B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111307564_111307565insCTAG , CM000668.2:g.111307564_111307565insCTAG	GRCh38
NC_000006.11:g.111628767_111628768insCTAG , CM000668.1:g.111628767_111628768insCTAG	GRCh37
NC_000006.10:g.111735460_111735461insCTAG	NCBI36
NG_053000.1:g.181151_181152insCTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368802.8:c.9048_9049insCTAG (REV3L) MANE Select	ENSP00000357792.3:p.Lys3017LeufsTer10
ENST00000666581.2:n.277+29406_277+29407insCTAG (MFSD4B)
ENST00000673245.1:n.273+11789_273+11790insCTAG (MFSD4B)
ENST00000673446.1:n.179+39727_179+39728insCTAG (MFSD4B)
ENST00000358835.7:c.9048_9049insCTAG (REV3L)	ENSP00000351697.3:p.Lys3017LeufsTer10
ENST00000368802.7:c.9048_9049insCTAG (REV3L)	ENSP00000357792.3:p.Lys3017LeufsTer10
ENST00000368805.5:c.9048_9049insCTAG (REV3L)	ENSP00000357795.1:p.Lys3017LeufsTer10
ENST00000422377.5:c.*9032_*9033insCTAG (REV3L)	ENSP00000393184.1:n.*9032_*9033insCTAG
ENST00000434009.5:c.*9139_*9140insCTAG (REV3L)	ENSP00000391605.1:n.*9139_*9140insCTAG
ENST00000435970.5:c.8814_8815insCTAG (REV3L)	ENSP00000402003.1:p.Lys2939LeufsTer10
ENST00000462119.5:n.1185_1186insCTAG (REV3L)
NM_001286431.1:c.8814_8815insCTAG (REV3L)	NP_001273360.1:p.Lys2939LeufsTer10
NM_001286432.1:c.8814_8815insCTAG (REV3L)	NP_001273361.1:p.Lys2939LeufsTer10
NM_002912.4:c.9048_9049insCTAG (REV3L)	NP_002903.3:p.Lys3017LeufsTer10
XM_006715543.2:c.9048_9049insCTAG (REV3L)	XP_006715606.1:p.Lys3017LeufsTer10
XM_006715544.2:c.8814_8815insCTAG (REV3L)	XP_006715607.1:p.Lys2939LeufsTer10
XM_011536028.1:c.9129_9130insCTAG (REV3L)	XP_011534330.1:p.Lys3044LeufsTer10
XM_011536029.1:c.9126_9127insCTAG (REV3L)	XP_011534331.1:p.Lys3043LeufsTer10
XM_011536030.1:c.9051_9052insCTAG (REV3L)	XP_011534332.1:p.Lys3018LeufsTer10
XM_011536031.1:c.8895_8896insCTAG (REV3L)	XP_011534333.1:p.Lys2966LeufsTer10
XM_011536032.1:c.8895_8896insCTAG (REV3L)	XP_011534334.1:p.Lys2966LeufsTer10
XR_942871.1:n.2045+29406_2045+29407insCTAG
XM_011536028.2:c.9129_9130insCTAG (REV3L)	XP_011534330.1:p.Lys3044LeufsTer10
XM_011536029.3:c.9126_9127insCTAG (REV3L)	XP_011534331.1:p.Lys3043LeufsTer10
XM_011536030.3:c.9051_9052insCTAG (REV3L)	XP_011534332.1:p.Lys3018LeufsTer10
XM_011536031.3:c.8895_8896insCTAG (REV3L)	XP_011534333.1:p.Lys2966LeufsTer10
XM_011536032.2:c.8895_8896insCTAG (REV3L)	XP_011534334.1:p.Lys2966LeufsTer10
XM_017011152.2:c.8892_8893insCTAG (REV3L)	XP_016866641.1:p.Lys2965LeufsTer10
XM_017011153.1:c.8892_8893insCTAG (REV3L)	XP_016866642.1:p.Lys2965LeufsTer10
XM_017011154.1:c.8892_8893insCTAG (REV3L)	XP_016866643.1:p.Lys2965LeufsTer10
XR_001743550.2:n.9234_9235insCTAG (REV3L)
XR_001743552.2:n.9156_9157insCTAG (REV3L)
XR_001743553.2:n.9552_9553insCTAG (REV3L)
XR_001743555.2:n.9474_9475insCTAG (REV3L)
XR_001743556.2:n.9281_9282insCTAG (REV3L)
XR_002956293.1:n.10492_10493insCTAG (REV3L)
NM_001286431.2:c.8814_8815insCTAG (REV3L)	NP_001273360.1:p.Lys2939LeufsTer10
NM_001372078.1:c.9048_9049insCTAG (REV3L) MANE Select	NP_001359007.1:p.Lys3017LeufsTer10
NM_001286432.2:c.8814_8815insCTAG (REV3L)	NP_001273361.1:p.Lys2939LeufsTer10
NM_002912.5:c.9048_9049insCTAG (REV3L)	NP_002903.3:p.Lys3017LeufsTer10