Canonical Allele Identifier: CA406361990

Gene: ERCC2

Linked Data

• dbSNP Id: rs1971828683
• MyVariant Identifiers: chr19:g.45855499A>G (hg19) ; chr19:g.45352241A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352241A>G , CM000681.2:g.45352241A>G	GRCh38
NC_000019.9:g.45855499A>G , CM000681.1:g.45855499A>G	GRCh37
NC_000019.8:g.50547339A>G	NCBI36
NG_007067.2:g.23347T>C , LRG_461:g.23347T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000391944.8:c.2158T>C	ENSP00000375808.4:p.Phe720Leu
ENST00000682414.1:c.2158T>C	ENSP00000507019.1:p.Phe720Leu
ENST00000682508.1:n.2187T>C
ENST00000684218.1:c.*1416T>C	ENSP00000507804.1:n.*1416T>C
ENST00000684264.1:n.1714T>C
ENST00000684407.1:c.2035T>C	ENSP00000507775.1:p.Phe679Leu
ENST00000684458.1:c.*644T>C	ENSP00000508260.1:n.*644T>C
ENST00000684468.1:n.1870T>C
ENST00000391945.10:c.2158T>C MANE Select	ENSP00000375809.4:p.Phe720Leu
ENST00000646507.1:n.2255T>C
ENST00000391941.6:c.2086T>C	ENSP00000375805.2:p.Phe696Leu
ENST00000391942.6:n.1329T>C
ENST00000391944.7:c.1924T>C	ENSP00000375808.3:p.Phe642Leu
ENST00000391945.8:c.2158T>C	ENSP00000375809.3:p.Phe720Leu
ENST00000588652.5:n.2246T>C
NM_000400.3:c.2158T>C , LRG_461t1:c.2158T>C	NP_000391.1:p.Phe720Leu
XM_011526611.1:c.2080T>C	XP_011524913.1:p.Phe694Leu
XM_011526611.2:c.2080T>C	XP_011524913.1:p.Phe694Leu
XM_017026467.1:c.2035T>C	XP_016881956.1:p.Phe679Leu
XR_001753633.2:n.2205T>C
XR_001753634.2:n.2141T>C
NM_000400.4:c.2158T>C MANE Select	NP_000391.1:p.Phe720Leu