Canonical Allele Identifier: CA406360814

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45855465A>G (hg19) ; chr19:g.45352207A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352207A>G , CM000681.2:g.45352207A>G	GRCh38
NC_000019.9:g.45855465A>G , CM000681.1:g.45855465A>G	GRCh37
NC_000019.8:g.50547305A>G	NCBI36
NG_007067.2:g.23381T>C , LRG_461:g.23381T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.2192T>C	ENSP00000375808.4:p.Val731Ala
ENST00000682414.1:c.2190+2T>C	ENSP00000507019.1:n.2190+2T>C
ENST00000682508.1:n.2219+2T>C
ENST00000684218.1:c.*1448+2T>C	ENSP00000507804.1:n.*1448+2T>C
ENST00000684264.1:n.1746+2T>C
ENST00000684407.1:c.2067+2T>C	ENSP00000507775.1:n.2067+2T>C
ENST00000684458.1:c.*676+2T>C	ENSP00000508260.1:n.*676+2T>C
ENST00000684468.1:n.1902+2T>C
ENST00000391945.10:c.2190+2T>C MANE Select	ENSP00000375809.4:n.2190+2T>C
ENST00000646507.1:n.2287+2T>C
ENST00000391942.6:n.1361+2T>C
ENST00000391944.7:c.1956+2T>C	ENSP00000375808.3:n.1956+2T>C
ENST00000391945.8:c.2190+2T>C	ENSP00000375809.3:n.2190+2T>C
ENST00000588652.5:n.2278+2T>C
NM_000400.3:c.2190+2T>C , LRG_461t1:c.2190+2T>C	NP_000391.1:n.2190+2T>C
XM_011526611.1:c.2112+2T>C	XP_011524913.1:n.2112+2T>C
XM_011526611.2:c.2112+2T>C	XP_011524913.1:n.2112+2T>C
XM_017026467.1:c.2067+2T>C	XP_016881956.1:n.2067+2T>C
XR_001753633.2:n.2237+2T>C
XR_001753634.2:n.2173+2T>C
NM_000400.4:c.2190+2T>C MANE Select	NP_000391.1:n.2190+2T>C