Canonical Allele Identifier: CA2585786673

Gene: ERCC2

Linked Data

• gnomAD v4: 19-45357406-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45357406C>T , CM000681.2:g.45357406C>T	GRCh38
NC_000019.9:g.45860664C>T , CM000681.1:g.45860664C>T	GRCh37
NC_000019.8:g.50552504C>T	NCBI36
NG_007067.2:g.18182G>A , LRG_461:g.18182G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1378-35G>A	ENSP00000375808.4:n.1378-35G>A
ENST00000682414.1:c.1378-35G>A	ENSP00000507019.1:n.1378-35G>A
ENST00000682508.1:n.1407-35G>A
ENST00000684218.1:c.*636-35G>A	ENSP00000507804.1:n.*636-35G>A
ENST00000684264.1:n.934-35G>A
ENST00000684407.1:c.1255-35G>A	ENSP00000507775.1:n.1255-35G>A
ENST00000684458.1:c.1308-35G>A	ENSP00000508260.1:n.1308-35G>A
ENST00000684468.1:n.1154-35G>A
ENST00000391945.10:c.1378-35G>A MANE Select	ENSP00000375809.4:n.1378-35G>A
ENST00000587376.6:c.501-35G>A
ENST00000646507.1:n.1475-35G>A
ENST00000391941.6:c.1306-35G>A	ENSP00000375805.2:n.1306-35G>A
ENST00000391942.6:n.549-35G>A
ENST00000391944.7:c.1144-35G>A	ENSP00000375808.3:n.1144-35G>A
ENST00000391945.8:c.1378-35G>A	ENSP00000375809.3:n.1378-35G>A
ENST00000587376.5:c.501-35G>A
ENST00000588652.5:n.1466-35G>A
NM_000400.3:c.1378-35G>A , LRG_461t1:c.1378-35G>A	NP_000391.1:n.1378-35G>A
XM_011526611.1:c.1300-35G>A	XP_011524913.1:n.1300-35G>A
XR_935763.1:n.1425-35G>A
XM_011526611.2:c.1300-35G>A	XP_011524913.1:n.1300-35G>A
XM_017026467.1:c.1255-35G>A	XP_016881956.1:n.1255-35G>A
XR_001753633.2:n.1425-35G>A
XR_001753634.2:n.1425-35G>A
NM_000400.4:c.1378-35G>A MANE Select	NP_000391.1:n.1378-35G>A