Canonical Allele Identifier: CA2585785961

Gene: ERCC2

Linked Data

• gnomAD v4: 19-45353425-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45353425T>C , CM000681.2:g.45353425T>C	GRCh38
NC_000019.9:g.45856683T>C , CM000681.1:g.45856683T>C	GRCh37
NC_000019.8:g.50548523T>C	NCBI36
NG_007067.2:g.22163A>G , LRG_461:g.22163A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1666-91A>G	ENSP00000375808.4:n.1666-91A>G
ENST00000682414.1:c.1666-91A>G	ENSP00000507019.1:n.1666-91A>G
ENST00000682508.1:n.1695-91A>G
ENST00000684218.1:c.*924-91A>G	ENSP00000507804.1:n.*924-91A>G
ENST00000684264.1:n.1222-91A>G
ENST00000684407.1:c.1543-91A>G	ENSP00000507775.1:n.1543-91A>G
ENST00000684458.1:c.*152-91A>G	ENSP00000508260.1:n.*152-91A>G
ENST00000684468.1:n.1378-91A>G
ENST00000391945.10:c.1666-91A>G MANE Select	ENSP00000375809.4:n.1666-91A>G
ENST00000587376.6:c.725-91A>G
ENST00000646507.1:n.1763-91A>G
ENST00000391941.6:c.1594-91A>G	ENSP00000375805.2:n.1594-91A>G
ENST00000391942.6:n.837-91A>G
ENST00000391944.7:c.1432-91A>G	ENSP00000375808.3:n.1432-91A>G
ENST00000391945.8:c.1666-91A>G	ENSP00000375809.3:n.1666-91A>G
ENST00000587376.5:c.725-91A>G
ENST00000588652.5:n.1754-91A>G
NM_000400.3:c.1666-91A>G , LRG_461t1:c.1666-91A>G	NP_000391.1:n.1666-91A>G
XM_011526611.1:c.1588-91A>G	XP_011524913.1:n.1588-91A>G
XR_935763.1:n.1649-91A>G
XM_011526611.2:c.1588-91A>G	XP_011524913.1:n.1588-91A>G
XM_017026467.1:c.1543-91A>G	XP_016881956.1:n.1543-91A>G
XR_001753633.2:n.1713-91A>G
XR_001753634.2:n.1649-91A>G
NM_000400.4:c.1666-91A>G MANE Select	NP_000391.1:n.1666-91A>G