Canonical Allele Identifier: CA406362721

Gene: ERCC2

Linked Data

• ClinVar Variation Id: 1784849
• ClinVar RCV Id: RCV002419878
• gnomAD v4: 19-45352514-C-T
• MyVariant Identifiers: chr19:g.45855772C>T (hg19) ; chr19:g.45352514C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352514C>T , CM000681.2:g.45352514C>T	GRCh38
NC_000019.9:g.45855772C>T , CM000681.1:g.45855772C>T	GRCh37
NC_000019.8:g.50547612C>T	NCBI36
NG_007067.2:g.23074G>A , LRG_461:g.23074G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000391944.8:c.2038G>A	ENSP00000375808.4:p.Ala680Thr
ENST00000682414.1:c.2038G>A	ENSP00000507019.1:p.Ala680Thr
ENST00000682508.1:n.2067G>A
ENST00000684218.1:c.*1296G>A	ENSP00000507804.1:n.*1296G>A
ENST00000684264.1:n.1594G>A
ENST00000684407.1:c.1915G>A	ENSP00000507775.1:p.Ala639Thr
ENST00000684458.1:c.*524G>A	ENSP00000508260.1:n.*524G>A
ENST00000684468.1:n.1750G>A
ENST00000391945.10:c.2038G>A MANE Select	ENSP00000375809.4:p.Ala680Thr
ENST00000646507.1:n.2135G>A
ENST00000391941.6:c.1966G>A	ENSP00000375805.2:p.Ala656Thr
ENST00000391942.6:n.1209G>A
ENST00000391944.7:c.1804G>A	ENSP00000375808.3:p.Ala602Thr
ENST00000391945.8:c.2038G>A	ENSP00000375809.3:p.Ala680Thr
ENST00000588652.5:n.2126G>A
NM_000400.3:c.2038G>A , LRG_461t1:c.2038G>A	NP_000391.1:p.Ala680Thr
XM_011526611.1:c.1960G>A	XP_011524913.1:p.Ala654Thr
XM_011526611.2:c.1960G>A	XP_011524913.1:p.Ala654Thr
XM_017026467.1:c.1915G>A	XP_016881956.1:p.Ala639Thr
XR_001753633.2:n.2085G>A
XR_001753634.2:n.2021G>A
NM_000400.4:c.2038G>A MANE Select	NP_000391.1:p.Ala680Thr