Canonical Allele Identifier: CA1093180928

Gene: REV3L

Linked Data

• dbSNP Id: rs1792474522
• gnomAD v3: 6-111473261-A-G
• gnomAD v4: 6-111473261-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111473261A>G , CM000668.2:g.111473261A>G	GRCh38
NC_000006.11:g.111794464A>G , CM000668.1:g.111794464A>G	GRCh37
NC_000006.10:g.111901157A>G	NCBI36
NG_053000.1:g.15455T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368802.8:c.139+9489T>C MANE Select	ENSP00000357792.3:n.139+9489T>C
ENST00000358835.7:c.139+9489T>C	ENSP00000351697.3:n.139+9489T>C
ENST00000368802.7:c.139+9489T>C	ENSP00000357792.3:n.139+9489T>C
ENST00000368805.5:c.139+9489T>C	ENSP00000357795.1:n.139+9489T>C
ENST00000422377.5:c.140-1121T>C	ENSP00000393184.1:n.140-1121T>C
ENST00000434009.5:c.140-1121T>C	ENSP00000391605.1:n.140-1121T>C
ENST00000435970.5:c.-223-1121T>C	ENSP00000402003.1:n.-223-1121T>C
NM_001286431.1:c.-330-1121T>C	NP_001273360.1:n.-330-1121T>C
NM_001286432.1:c.-223-1121T>C	NP_001273361.1:n.-223-1121T>C
NM_002912.4:c.139+9489T>C	NP_002903.3:n.139+9489T>C
XM_006715543.2:c.139+9489T>C	XP_006715606.1:n.139+9489T>C
XM_006715544.2:c.-223-1121T>C	XP_006715607.1:n.-223-1121T>C
XM_011536028.1:c.139+9489T>C	XP_011534330.1:n.139+9489T>C
XM_011536029.1:c.139+9489T>C	XP_011534331.1:n.139+9489T>C
XM_011536030.1:c.139+9489T>C	XP_011534332.1:n.139+9489T>C
XM_011536031.1:c.-223-1121T>C	XP_011534333.1:n.-223-1121T>C
XM_011536032.1:c.-224+985T>C	XP_011534334.1:n.-224+985T>C
XM_011536033.1:c.139+9489T>C	XP_011534335.1:n.139+9489T>C
XM_011536034.1:c.139+9489T>C	XP_011534336.1:n.139+9489T>C
XM_011536035.1:c.139+9489T>C	XP_011534337.1:n.139+9489T>C
XM_011536036.1:c.139+9489T>C	XP_011534338.1:n.139+9489T>C
XR_942545.1:n.688+9489T>C
XR_942546.1:n.688+9489T>C
XM_011536028.2:c.139+9489T>C	XP_011534330.1:n.139+9489T>C
XM_011536029.3:c.139+9489T>C	XP_011534331.1:n.139+9489T>C
XM_011536030.3:c.139+9489T>C	XP_011534332.1:n.139+9489T>C
XM_011536031.3:c.-223-1121T>C	XP_011534333.1:n.-223-1121T>C
XM_011536032.2:c.-224+985T>C	XP_011534334.1:n.-224+985T>C
XM_011536036.3:c.139+9489T>C	XP_011534338.1:n.139+9489T>C
XM_017011152.2:c.-223-1121T>C	XP_016866641.1:n.-223-1121T>C
XM_017011153.1:c.-224+985T>C	XP_016866642.1:n.-224+985T>C
XM_017011154.1:c.-223-1121T>C	XP_016866643.1:n.-223-1121T>C
XM_017011155.2:c.139+9489T>C	XP_016866644.1:n.139+9489T>C
XR_001743550.2:n.435+9489T>C
XR_001743552.2:n.435+9489T>C
XR_001743553.2:n.435+9489T>C
XR_001743554.2:n.435+9489T>C
XR_001743555.2:n.435+9489T>C
XR_001743556.2:n.435+9489T>C
XR_002956293.1:n.435+9489T>C
NM_001286431.2:c.-330-1121T>C	NP_001273360.1:n.-330-1121T>C
NM_001372078.1:c.139+9489T>C MANE Select	NP_001359007.1:n.139+9489T>C
NM_001286432.2:c.-223-1121T>C	NP_001273361.1:n.-223-1121T>C
NM_002912.5:c.139+9489T>C	NP_002903.3:n.139+9489T>C