Canonical Allele Identifier: CA15943508
Gene: ERCC1 HGNC NCBI
POLR1G HGNC NCBI

Linked Data

dbSNP Id: rs1046282

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45407414A>G , CM000681.2:g.45407414A>G GRCh38
NC_000019.9:g.45910672A>G , CM000681.1:g.45910672A>G GRCh37
NC_000019.8:g.50602512A>G NCBI36
NG_015839.2:g.76415T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000710953.1:c.*2494T>C (ERCC1) ENSP00000518553.1:n.*2494T>C
ENST00000300853.8:c.*2261T>C (ERCC1) MANE Select ENSP00000300853.3:n.*2261T>C
ENST00000309424.8:c.164+179A>G (POLR1G) MANE Select ENSP00000310966.3:n.164+179A>G
ENST00000300853.7:c.*2261T>C (ERCC1) ENSP00000300853.2:n.*2261T>C
ENST00000309424.7:c.164+179A>G (POLR1G) ENSP00000310966.3:n.164+179A>G
ENST00000423698.6:c.*2261T>C (ERCC1) ENSP00000394875.2:n.*2261T>C
ENST00000589804.1:c.170+179A>G (POLR1G) ENSP00000465099.1:n.170+179A>G
ENST00000590794.1:c.20+696A>G (POLR1G)
ENST00000592852.1:c.-371+179A>G (POLR1G) ENSP00000467771.1:n.-371+179A>G
NM_001166049.1:c.*2261T>C (ERCC1) NP_001159521.1:n.*2261T>C
NM_001297590.1:c.170+179A>G (POLR1G) NP_001284519.1:n.170+179A>G
NM_001983.3:c.*2261T>C (ERCC1) NP_001974.1:n.*2261T>C
NM_012099.1:c.164+179A>G (POLR1G) NP_036231.1:n.164+179A>G
XM_017026460.2:c.*2261T>C (ERCC1) XP_016881949.1:n.*2261T>C
XM_017026461.1:c.*2261T>C (ERCC1) XP_016881950.1:n.*2261T>C
XM_017026462.1:c.*2261T>C (ERCC1) XP_016881951.1:n.*2261T>C
XM_017026463.1:c.*2261T>C (ERCC1) XP_016881952.1:n.*2261T>C
XM_017026464.1:c.*2261T>C (ERCC1) XP_016881953.1:n.*2261T>C
XM_017026465.1:c.*2261T>C (ERCC1) XP_016881954.1:n.*2261T>C
XM_017026466.1:c.*2261T>C (ERCC1) XP_016881955.1:n.*2261T>C
XR_001753631.1:n.3741T>C (ERCC1)
XR_001753632.1:n.4211T>C (ERCC1)
NM_001166049.2:c.*2261T>C (ERCC1) NP_001159521.1:n.*2261T>C
NM_001297590.2:c.170+179A>G (POLR1G) NP_001284519.1:n.170+179A>G
NM_001369412.1:c.*2261T>C (ERCC1) NP_001356341.1:n.*2261T>C
NM_001369413.1:c.*2261T>C (ERCC1) NP_001356342.1:n.*2261T>C
NM_001369414.1:c.*2261T>C (ERCC1) NP_001356343.1:n.*2261T>C
NM_001369415.1:c.*2261T>C (ERCC1) NP_001356344.1:n.*2261T>C
NM_001369416.1:c.*2261T>C (ERCC1) NP_001356345.1:n.*2261T>C
NM_001369417.1:c.*2261T>C (ERCC1) NP_001356346.1:n.*2261T>C
NM_001369418.1:c.*2261T>C (ERCC1) NP_001356347.1:n.*2261T>C
NM_001369419.1:c.*2261T>C (ERCC1) NP_001356348.1:n.*2261T>C
NM_001983.4:c.*2261T>C (ERCC1) MANE Select NP_001974.1:n.*2261T>C
NM_012099.2:c.164+179A>G (POLR1G) NP_036231.1:n.164+179A>G
NM_001297590.3:c.170+179A>G (POLR1G) NP_001284519.1:n.170+179A>G
NM_012099.3:c.164+179A>G (POLR1G) MANE Select NP_036231.1:n.164+179A>G