Canonical Allele Identifier: CA406363895

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45856057C>G (hg19) ; chr19:g.45352799C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352799C>G , CM000681.2:g.45352799C>G	GRCh38
NC_000019.9:g.45856057C>G , CM000681.1:g.45856057C>G	GRCh37
NC_000019.8:g.50547897C>G	NCBI36
NG_007067.2:g.22789G>C , LRG_461:g.22789G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1849G>C	ENSP00000375808.4:p.Ala617Pro
ENST00000682414.1:c.1849G>C	ENSP00000507019.1:p.Ala617Pro
ENST00000682508.1:n.1878G>C
ENST00000684218.1:c.*1107G>C	ENSP00000507804.1:n.*1107G>C
ENST00000684264.1:n.1405G>C
ENST00000684407.1:c.1726G>C	ENSP00000507775.1:p.Ala576Pro
ENST00000684458.1:c.*335G>C	ENSP00000508260.1:n.*335G>C
ENST00000684468.1:n.1561G>C
ENST00000391945.10:c.1849G>C MANE Select	ENSP00000375809.4:p.Ala617Pro
ENST00000646507.1:n.1946G>C
ENST00000391941.6:c.1777G>C	ENSP00000375805.2:p.Ala593Pro
ENST00000391942.6:n.1020G>C
ENST00000391944.7:c.1615G>C	ENSP00000375808.3:p.Ala539Pro
ENST00000391945.8:c.1849G>C	ENSP00000375809.3:p.Ala617Pro
ENST00000588652.5:n.1937G>C
NM_000400.3:c.1849G>C , LRG_461t1:c.1849G>C	NP_000391.1:p.Ala617Pro
XM_011526611.1:c.1771G>C	XP_011524913.1:p.Ala591Pro
XM_011526611.2:c.1771G>C	XP_011524913.1:p.Ala591Pro
XM_017026467.1:c.1726G>C	XP_016881956.1:p.Ala576Pro
XR_001753633.2:n.1896G>C
XR_001753634.2:n.1832G>C
NM_000400.4:c.1849G>C MANE Select	NP_000391.1:p.Ala617Pro