Canonical Allele Identifier: CA406369793

Gene: ERCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45361531G>C , CM000681.2:g.45361531G>C	GRCh38
NC_000019.9:g.45864789G>C , CM000681.1:g.45864789G>C	GRCh37
NC_000019.8:g.50556629G>C	NCBI36
NG_007067.2:g.14057C>G , LRG_461:g.14057C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000400.4:c.1230C>G MANE Select	NP_000391.1:p.Tyr410Ter
ENST00000391945.10:c.1230C>G MANE Select	ENSP00000375809.4:p.Tyr410Ter
NM_000400.3:c.1230C>G , LRG_461t1:c.1230C>G	NP_000391.1:p.Tyr410Ter
NM_001130867.1:c.1158C>G	NP_001124339.1:p.Tyr386Ter
NM_001130867.2:c.1158C>G	NP_001124339.1:p.Tyr386Ter
ENST00000391941.6:c.1158C>G	ENSP00000375805.2:p.Tyr386Ter
ENST00000391942.6:n.401C>G
ENST00000391944.7:c.996C>G	ENSP00000375808.3:p.Tyr332Ter
ENST00000391944.8:c.1230C>G	ENSP00000375808.4:p.Tyr410Ter
ENST00000391945.8:c.1230C>G	ENSP00000375809.3:p.Tyr410Ter
ENST00000485403.6:c.1158C>G	ENSP00000431229.2:p.Tyr386Ter
ENST00000587376.5:c.353C>G
ENST00000587376.6:c.353C>G
ENST00000646507.1:n.1327C>G
ENST00000682414.1:c.1230C>G	ENSP00000507019.1:p.Tyr410Ter
ENST00000682508.1:n.1259C>G
ENST00000684218.1:c.*488C>G	ENSP00000507804.1:n.*488C>G
ENST00000684407.1:c.1107C>G	ENSP00000507775.1:p.Tyr369Ter
ENST00000684458.1:c.1230C>G	ENSP00000508260.1:p.Tyr410Ter
XM_011526611.1:c.1152C>G	XP_011524913.1:p.Tyr384Ter
XM_011526611.2:c.1152C>G	XP_011524913.1:p.Tyr384Ter
XM_017026467.1:c.1107C>G	XP_016881956.1:p.Tyr369Ter
XR_001753633.2:n.1277C>G
XR_001753634.2:n.1277C>G
XR_935763.1:n.1277C>G