Canonical Allele Identifier: CA633335061

Gene: ERCC1 POLR1G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45409895_45409897del , CM000681.2:g.45409895_45409897del	GRCh38
NC_000019.9:g.45913153_45913155del , CM000681.1:g.45913153_45913155del	GRCh37
NC_000019.8:g.50604993_50604995del	NCBI36
NG_015839.2:g.73949_73951del

Transcript Alleles

HGVS	Amino-acid Change
NM_001983.4:c.844-155_844-153del (ERCC1) MANE Select	NP_001974.1:n.844-155_844-153del
NM_012099.3:c.*394_*396del (POLR1G) MANE Select	NP_036231.1:n.*394_*396del
ENST00000300853.8:c.844-155_844-153del (ERCC1) MANE Select	ENSP00000300853.3:n.844-155_844-153del
ENST00000309424.8:c.*394_*396del (POLR1G) MANE Select	ENSP00000310966.3:n.*394_*396del
NM_001166049.1:c.772-155_772-153del (ERCC1)	NP_001159521.1:n.772-155_772-153del
NM_001166049.2:c.772-155_772-153del (ERCC1)	NP_001159521.1:n.772-155_772-153del
NM_001297590.1:c.*394_*396del (POLR1G)	NP_001284519.1:n.*394_*396del
NM_001297590.2:c.*394_*396del (POLR1G)	NP_001284519.1:n.*394_*396del
NM_001297590.3:c.*394_*396del (POLR1G)	NP_001284519.1:n.*394_*396del
NM_001369412.1:c.844-155_844-153del (ERCC1)	NP_001356341.1:n.844-155_844-153del
NM_001369413.1:c.844-155_844-153del (ERCC1)	NP_001356342.1:n.844-155_844-153del
NM_001369414.1:c.844-155_844-153del (ERCC1)	NP_001356343.1:n.844-155_844-153del
NM_001369415.1:c.844-155_844-153del (ERCC1)	NP_001356344.1:n.844-155_844-153del
NM_001369416.1:c.844-155_844-153del (ERCC1)	NP_001356345.1:n.844-155_844-153del
NM_001369417.1:c.772-155_772-153del (ERCC1)	NP_001356346.1:n.772-155_772-153del
NM_001369418.1:c.772-155_772-153del (ERCC1)	NP_001356347.1:n.772-155_772-153del
NM_001369419.1:c.772-155_772-153del (ERCC1)	NP_001356348.1:n.772-155_772-153del
NM_001983.3:c.844-155_844-153del (ERCC1)	NP_001974.1:n.844-155_844-153del
NM_012099.1:c.*394_*396del (POLR1G)	NP_036231.1:n.*394_*396del
NM_012099.2:c.*394_*396del (POLR1G)	NP_036231.1:n.*394_*396del
ENST00000300853.7:c.844-155_844-153del (ERCC1)	ENSP00000300853.2:n.844-155_844-153del
ENST00000309424.7:c.*394_*396del (POLR1G)	ENSP00000310966.3:n.*394_*396del
ENST00000340192.11:c.772-155_772-153del (ERCC1)	ENSP00000345203.6:n.772-155_772-153del
ENST00000423698.6:c.628-155_628-153del (ERCC1)	ENSP00000394875.2:n.628-155_628-153del
ENST00000588738.5:n.407-155_407-153del (ERCC1)
ENST00000589165.5:c.844-155_844-153del (ERCC1)	ENSP00000468035.1:n.844-155_844-153del
ENST00000590701.5:c.236-155_236-153del (ERCC1)
ENST00000591636.5:c.603-155_603-153del (ERCC1)	ENSP00000468119.1:n.603-155_603-153del
ENST00000710953.1:c.*183-155_*183-153del (ERCC1)	ENSP00000518553.1:n.*183-155_*183-153del
XM_017026460.2:c.844-155_844-153del (ERCC1)	XP_016881949.1:n.844-155_844-153del
XM_017026461.1:c.844-155_844-153del (ERCC1)	XP_016881950.1:n.844-155_844-153del
XM_017026462.1:c.844-155_844-153del (ERCC1)	XP_016881951.1:n.844-155_844-153del
XM_017026463.1:c.844-155_844-153del (ERCC1)	XP_016881952.1:n.844-155_844-153del
XM_017026464.1:c.844-155_844-153del (ERCC1)	XP_016881953.1:n.844-155_844-153del
XM_017026465.1:c.772-155_772-153del (ERCC1)	XP_016881954.1:n.772-155_772-153del
XM_017026466.1:c.772-155_772-153del (ERCC1)	XP_016881955.1:n.772-155_772-153del
XR_001753631.1:n.1430-155_1430-153del (ERCC1)
XR_001753632.1:n.1900-155_1900-153del (ERCC1)