Canonical Allele Identifier: CA1654866735

Gene: REV3L MFSD4B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111307139_111307141delinsAAC , CM000668.2:g.111307139_111307141delinsAAC	GRCh38
NC_000006.11:g.111628342_111628344delinsAAC , CM000668.1:g.111628342_111628344delinsAAC	GRCh37
NC_000006.10:g.111735035_111735037delinsAAC	NCBI36
NG_053000.1:g.181575_181577delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368802.8:c.9252+220_9252+222delinsGTT (REV3L) MANE Select	ENSP00000357792.3:n.9252+220_9252+222delinsGTT
ENST00000666581.2:n.277+28981_277+28983delinsAAC (MFSD4B)
ENST00000673245.1:n.273+11364_273+11366delinsAAC (MFSD4B)
ENST00000673446.1:n.179+39302_179+39304delinsAAC (MFSD4B)
ENST00000358835.7:c.9252+220_9252+222delinsGTT (REV3L)	ENSP00000351697.3:n.9252+220_9252+222delinsGTT
ENST00000368802.7:c.9252+220_9252+222delinsGTT (REV3L)	ENSP00000357792.3:n.9252+220_9252+222delinsGTT
ENST00000368805.5:c.9252+220_9252+222delinsGTT (REV3L)	ENSP00000357795.1:n.9252+220_9252+222delinsGTT
ENST00000422377.5:c.*9236+220_*9236+222delinsGTT (REV3L)	ENSP00000393184.1:n.*9236+220_*9236+222delinsGTT
ENST00000434009.5:c.*9343+220_*9343+222delinsGTT (REV3L)	ENSP00000391605.1:n.*9343+220_*9343+222delinsGTT
ENST00000435970.5:c.9018+220_9018+222delinsGTT (REV3L)	ENSP00000402003.1:n.9018+220_9018+222delinsGTT
ENST00000462119.5:n.1389+220_1389+222delinsGTT (REV3L)
NM_001286431.1:c.9018+220_9018+222delinsGTT (REV3L)	NP_001273360.1:n.9018+220_9018+222delinsGTT
NM_001286432.1:c.9018+220_9018+222delinsGTT (REV3L)	NP_001273361.1:n.9018+220_9018+222delinsGTT
NM_002912.4:c.9252+220_9252+222delinsGTT (REV3L)	NP_002903.3:n.9252+220_9252+222delinsGTT
XM_006715543.2:c.9252+220_9252+222delinsGTT (REV3L)	XP_006715606.1:n.9252+220_9252+222delinsGTT
XM_006715544.2:c.9018+220_9018+222delinsGTT (REV3L)	XP_006715607.1:n.9018+220_9018+222delinsGTT
XM_011536028.1:c.9333+220_9333+222delinsGTT (REV3L)	XP_011534330.1:n.9333+220_9333+222delinsGTT
XM_011536029.1:c.9330+220_9330+222delinsGTT (REV3L)	XP_011534331.1:n.9330+220_9330+222delinsGTT
XM_011536030.1:c.9255+220_9255+222delinsGTT (REV3L)	XP_011534332.1:n.9255+220_9255+222delinsGTT
XM_011536031.1:c.9099+220_9099+222delinsGTT (REV3L)	XP_011534333.1:n.9099+220_9099+222delinsGTT
XM_011536032.1:c.9099+220_9099+222delinsGTT (REV3L)	XP_011534334.1:n.9099+220_9099+222delinsGTT
XR_942871.1:n.2045+28981_2045+28983delinsAAC
XM_011536028.2:c.9333+220_9333+222delinsGTT (REV3L)	XP_011534330.1:n.9333+220_9333+222delinsGTT
XM_011536029.3:c.9330+220_9330+222delinsGTT (REV3L)	XP_011534331.1:n.9330+220_9330+222delinsGTT
XM_011536030.3:c.9255+220_9255+222delinsGTT (REV3L)	XP_011534332.1:n.9255+220_9255+222delinsGTT
XM_011536031.3:c.9099+220_9099+222delinsGTT (REV3L)	XP_011534333.1:n.9099+220_9099+222delinsGTT
XM_011536032.2:c.9099+220_9099+222delinsGTT (REV3L)	XP_011534334.1:n.9099+220_9099+222delinsGTT
XM_017011152.2:c.9096+220_9096+222delinsGTT (REV3L)	XP_016866641.1:n.9096+220_9096+222delinsGTT
XM_017011153.1:c.9096+220_9096+222delinsGTT (REV3L)	XP_016866642.1:n.9096+220_9096+222delinsGTT
XM_017011154.1:c.9096+220_9096+222delinsGTT (REV3L)	XP_016866643.1:n.9096+220_9096+222delinsGTT
XR_001743550.2:n.9438+220_9438+222delinsGTT (REV3L)
XR_001743552.2:n.9360+220_9360+222delinsGTT (REV3L)
XR_001743553.2:n.9756+220_9756+222delinsGTT (REV3L)
XR_001743555.2:n.9678+220_9678+222delinsGTT (REV3L)
XR_001743556.2:n.9485+220_9485+222delinsGTT (REV3L)
XR_002956293.1:n.10696+220_10696+222delinsGTT (REV3L)
NM_001286431.2:c.9018+220_9018+222delinsGTT (REV3L)	NP_001273360.1:n.9018+220_9018+222delinsGTT
NM_001372078.1:c.9252+220_9252+222delinsGTT (REV3L) MANE Select	NP_001359007.1:n.9252+220_9252+222delinsGTT
NM_001286432.2:c.9018+220_9018+222delinsGTT (REV3L)	NP_001273361.1:n.9018+220_9018+222delinsGTT
NM_002912.5:c.9252+220_9252+222delinsGTT (REV3L)	NP_002903.3:n.9252+220_9252+222delinsGTT