Canonical Allele Identifier: CA2585785988

Gene: ERCC2

Linked Data

• gnomAD v4: 19-45353443-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45353444del , CM000681.2:g.45353444del	GRCh38
NC_000019.9:g.45856702del , CM000681.1:g.45856702del	GRCh37
NC_000019.8:g.50548542del	NCBI36
NG_007067.2:g.22144del , LRG_461:g.22144del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1666-110del	ENSP00000375808.4:n.1666-110del
ENST00000682414.1:c.1666-110del	ENSP00000507019.1:n.1666-110del
ENST00000682508.1:n.1695-110del
ENST00000684218.1:c.*924-110del	ENSP00000507804.1:n.*924-110del
ENST00000684264.1:n.1222-110del
ENST00000684407.1:c.1543-110del	ENSP00000507775.1:n.1543-110del
ENST00000684458.1:c.*152-110del	ENSP00000508260.1:n.*152-110del
ENST00000684468.1:n.1378-110del
ENST00000391945.10:c.1666-110del MANE Select	ENSP00000375809.4:n.1666-110del
ENST00000587376.6:c.725-110del
ENST00000646507.1:n.1763-110del
ENST00000391941.6:c.1594-110del	ENSP00000375805.2:n.1594-110del
ENST00000391942.6:n.837-110del
ENST00000391944.7:c.1432-110del	ENSP00000375808.3:n.1432-110del
ENST00000391945.8:c.1666-110del	ENSP00000375809.3:n.1666-110del
ENST00000587376.5:c.725-110del
ENST00000588652.5:n.1754-110del
NM_000400.3:c.1666-110del , LRG_461t1:c.1666-110del	NP_000391.1:n.1666-110del
XM_011526611.1:c.1588-110del	XP_011524913.1:n.1588-110del
XR_935763.1:n.1649-110del
XM_011526611.2:c.1588-110del	XP_011524913.1:n.1588-110del
XM_017026467.1:c.1543-110del	XP_016881956.1:n.1543-110del
XR_001753633.2:n.1713-110del
XR_001753634.2:n.1649-110del
NM_000400.4:c.1666-110del MANE Select	NP_000391.1:n.1666-110del