Canonical Allele Identifier: CA507953612

Gene: ERCC2

Linked Data

• ClinVar Variation Id: 2452338
• ClinVar RCV Id: RCV003172432
• gnomAD v4: 19-45364080-G-A
• MyVariant Identifiers: chr19:g.45867338G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45364080G>A , CM000681.2:g.45364080G>A	GRCh38
NC_000019.9:g.45867338G>A , CM000681.1:g.45867338G>A	GRCh37
NC_000019.8:g.50559178G>A	NCBI36
NG_007067.2:g.11508C>T , LRG_461:g.11508C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.855C>T	ENSP00000375808.4:p.Tyr285=
ENST00000682414.1:c.855C>T	ENSP00000507019.1:p.Tyr285=
ENST00000682508.1:n.884C>T
ENST00000684218.1:c.*113C>T	ENSP00000507804.1:n.*113C>T
ENST00000684407.1:c.732C>T	ENSP00000507775.1:p.Tyr244=
ENST00000684458.1:c.855C>T	ENSP00000508260.1:p.Tyr285=
ENST00000391945.10:c.855C>T MANE Select	ENSP00000375809.4:p.Tyr285=
ENST00000586131.6:c.783C>T	ENSP00000464887.1:p.Tyr261=
ENST00000646507.1:n.952C>T
ENST00000391941.6:c.783C>T	ENSP00000375805.2:p.Tyr261=
ENST00000391944.7:c.621C>T	ENSP00000375808.3:p.Tyr207=
ENST00000391945.8:c.855C>T	ENSP00000375809.3:p.Tyr285=
ENST00000485403.6:c.783C>T	ENSP00000431229.2:p.Tyr261=
ENST00000586131.5:c.783C>T	ENSP00000464887.1:p.Tyr261=
ENST00000591309.5:c.*113C>T	ENSP00000465207.1:n.*113C>T
NM_000400.3:c.855C>T , LRG_461t1:c.855C>T	NP_000391.1:p.Tyr285=
NM_001130867.1:c.783C>T	NP_001124339.1:p.Tyr261=
XM_011526611.1:c.777C>T	XP_011524913.1:p.Tyr259=
XR_935763.1:n.902C>T
XM_011526611.2:c.777C>T	XP_011524913.1:p.Tyr259=
XM_017026467.1:c.732C>T	XP_016881956.1:p.Tyr244=
XR_001753633.2:n.902C>T
XR_001753634.2:n.902C>T
NM_000400.4:c.855C>T MANE Select	NP_000391.1:p.Tyr285=
NM_001130867.2:c.783C>T	NP_001124339.1:p.Tyr261=