Canonical Allele Identifier: CA406367213

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45860604G>C (hg19) ; chr19:g.45357346G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45357346G>C , CM000681.2:g.45357346G>C	GRCh38
NC_000019.9:g.45860604G>C , CM000681.1:g.45860604G>C	GRCh37
NC_000019.8:g.50552444G>C	NCBI36
NG_007067.2:g.18242C>G , LRG_461:g.18242C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1403C>G	ENSP00000375808.4:p.Pro468Arg
ENST00000682414.1:c.1403C>G	ENSP00000507019.1:p.Pro468Arg
ENST00000682508.1:n.1432C>G
ENST00000684218.1:c.*661C>G	ENSP00000507804.1:n.*661C>G
ENST00000684264.1:n.959C>G
ENST00000684407.1:c.1280C>G	ENSP00000507775.1:p.Pro427Arg
ENST00000684458.1:c.1333C>G	ENSP00000508260.1:p.Pro445Ala
ENST00000684468.1:n.1179C>G
ENST00000391945.10:c.1403C>G MANE Select	ENSP00000375809.4:p.Pro468Arg
ENST00000587376.6:c.526C>G
ENST00000646507.1:n.1500C>G
ENST00000391941.6:c.1331C>G	ENSP00000375805.2:p.Pro444Arg
ENST00000391942.6:n.574C>G
ENST00000391944.7:c.1169C>G	ENSP00000375808.3:p.Pro390Arg
ENST00000391945.8:c.1403C>G	ENSP00000375809.3:p.Pro468Arg
ENST00000587376.5:c.526C>G
ENST00000588652.5:n.1491C>G
NM_000400.3:c.1403C>G , LRG_461t1:c.1403C>G	NP_000391.1:p.Pro468Arg
XM_011526611.1:c.1325C>G	XP_011524913.1:p.Pro442Arg
XR_935763.1:n.1450C>G
XM_011526611.2:c.1325C>G	XP_011524913.1:p.Pro442Arg
XM_017026467.1:c.1280C>G	XP_016881956.1:p.Pro427Arg
XR_001753633.2:n.1450C>G
XR_001753634.2:n.1450C>G
NM_000400.4:c.1403C>G MANE Select	NP_000391.1:p.Pro468Arg