Canonical Allele Identifier: CA507953541

Gene: ERCC2

Linked Data

• gnomAD v4: 19-45364041-G-T
• MyVariant Identifiers: chr19:g.45867299G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45364041G>T , CM000681.2:g.45364041G>T	GRCh38
NC_000019.9:g.45867299G>T , CM000681.1:g.45867299G>T	GRCh37
NC_000019.8:g.50559139G>T	NCBI36
NG_007067.2:g.11547C>A , LRG_461:g.11547C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.894C>A	ENSP00000375808.4:p.Ala298=
ENST00000682414.1:c.894C>A	ENSP00000507019.1:p.Ala298=
ENST00000682508.1:n.923C>A
ENST00000684218.1:c.*152C>A	ENSP00000507804.1:n.*152C>A
ENST00000684407.1:c.771C>A	ENSP00000507775.1:p.Ala257=
ENST00000684458.1:c.894C>A	ENSP00000508260.1:p.Ala298=
ENST00000391945.10:c.894C>A MANE Select	ENSP00000375809.4:p.Ala298=
ENST00000586131.6:c.822C>A	ENSP00000464887.1:p.Ala274=
ENST00000587376.6:c.17C>A
ENST00000646507.1:n.991C>A
ENST00000391941.6:c.822C>A	ENSP00000375805.2:p.Ala274=
ENST00000391944.7:c.660C>A	ENSP00000375808.3:p.Ala220=
ENST00000391945.8:c.894C>A	ENSP00000375809.3:p.Ala298=
ENST00000485403.6:c.822C>A	ENSP00000431229.2:p.Ala274=
ENST00000586131.5:c.822C>A	ENSP00000464887.1:p.Ala274=
ENST00000587376.5:c.17C>A
ENST00000591309.5:c.*152C>A	ENSP00000465207.1:n.*152C>A
NM_000400.3:c.894C>A , LRG_461t1:c.894C>A	NP_000391.1:p.Ala298=
NM_001130867.1:c.822C>A	NP_001124339.1:p.Ala274=
XM_011526611.1:c.816C>A	XP_011524913.1:p.Ala272=
XR_935763.1:n.941C>A
XM_011526611.2:c.816C>A	XP_011524913.1:p.Ala272=
XM_017026467.1:c.771C>A	XP_016881956.1:p.Ala257=
XR_001753633.2:n.941C>A
XR_001753634.2:n.941C>A
NM_000400.4:c.894C>A MANE Select	NP_000391.1:p.Ala298=
NM_001130867.2:c.822C>A	NP_001124339.1:p.Ala274=