Canonical Allele Identifier: CA507953528

Gene: ERCC2

Linked Data

• ClinVar Variation Id: 1765568
• ClinVar RCV Id: RCV002378468
• dbSNP Id: rs1250320135
• gnomAD v3: 19-45364032-C-T
• gnomAD v4: 19-45364032-C-T
• MyVariant Identifiers: chr19:g.45867290C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45364032C>T , CM000681.2:g.45364032C>T	GRCh38
NC_000019.9:g.45867290C>T , CM000681.1:g.45867290C>T	GRCh37
NC_000019.8:g.50559130C>T	NCBI36
NG_007067.2:g.11556G>A , LRG_461:g.11556G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.903G>A	ENSP00000375808.4:p.Thr301=
ENST00000682414.1:c.903G>A	ENSP00000507019.1:p.Thr301=
ENST00000682508.1:n.932G>A
ENST00000684218.1:c.*161G>A	ENSP00000507804.1:n.*161G>A
ENST00000684407.1:c.780G>A	ENSP00000507775.1:p.Thr260=
ENST00000684458.1:c.903G>A	ENSP00000508260.1:p.Thr301=
ENST00000391945.10:c.903G>A MANE Select	ENSP00000375809.4:p.Thr301=
ENST00000586131.6:c.831G>A	ENSP00000464887.1:p.Thr277=
ENST00000587376.6:c.26G>A
ENST00000646507.1:n.1000G>A
ENST00000391941.6:c.831G>A	ENSP00000375805.2:p.Thr277=
ENST00000391944.7:c.669G>A	ENSP00000375808.3:p.Thr223=
ENST00000391945.8:c.903G>A	ENSP00000375809.3:p.Thr301=
ENST00000485403.6:c.831G>A	ENSP00000431229.2:p.Thr277=
ENST00000586131.5:c.831G>A	ENSP00000464887.1:p.Thr277=
ENST00000587376.5:c.26G>A
NM_000400.3:c.903G>A , LRG_461t1:c.903G>A	NP_000391.1:p.Thr301=
NM_001130867.1:c.831G>A	NP_001124339.1:p.Thr277=
XM_011526611.1:c.825G>A	XP_011524913.1:p.Thr275=
XR_935763.1:n.950G>A
XM_011526611.2:c.825G>A	XP_011524913.1:p.Thr275=
XM_017026467.1:c.780G>A	XP_016881956.1:p.Thr260=
XR_001753633.2:n.950G>A
XR_001753634.2:n.950G>A
NM_000400.4:c.903G>A MANE Select	NP_000391.1:p.Thr301=
NM_001130867.2:c.831G>A	NP_001124339.1:p.Thr277=