Canonical Allele Identifier: CA406364508

Gene: ERCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45353316G>A , CM000681.2:g.45353316G>A	GRCh38
NC_000019.9:g.45856574G>A , CM000681.1:g.45856574G>A	GRCh37
NC_000019.8:g.50548414G>A	NCBI36
NG_007067.2:g.22272C>T , LRG_461:g.22272C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000400.4:c.1684C>T MANE Select	NP_000391.1:p.Gln562Ter
ENST00000391945.10:c.1684C>T MANE Select	ENSP00000375809.4:p.Gln562Ter
NM_000400.3:c.1684C>T , LRG_461t1:c.1684C>T	NP_000391.1:p.Gln562Ter
ENST00000391941.6:c.1612C>T	ENSP00000375805.2:p.Gln538Ter
ENST00000391942.6:n.855C>T
ENST00000391944.7:c.1450C>T	ENSP00000375808.3:p.Gln484Ter
ENST00000391944.8:c.1684C>T	ENSP00000375808.4:p.Gln562Ter
ENST00000391945.8:c.1684C>T	ENSP00000375809.3:p.Gln562Ter
ENST00000587376.5:c.743C>T
ENST00000587376.6:c.743C>T
ENST00000588652.5:n.1772C>T
ENST00000646507.1:n.1781C>T
ENST00000682414.1:c.1684C>T	ENSP00000507019.1:p.Gln562Ter
ENST00000682508.1:n.1713C>T
ENST00000684218.1:c.*942C>T	ENSP00000507804.1:n.*942C>T
ENST00000684264.1:n.1240C>T
ENST00000684407.1:c.1561C>T	ENSP00000507775.1:p.Gln521Ter
ENST00000684458.1:c.*170C>T	ENSP00000508260.1:n.*170C>T
ENST00000684468.1:n.1396C>T
XM_011526611.1:c.1606C>T	XP_011524913.1:p.Gln536Ter
XM_011526611.2:c.1606C>T	XP_011524913.1:p.Gln536Ter
XM_017026467.1:c.1561C>T	XP_016881956.1:p.Gln521Ter
XR_001753633.2:n.1731C>T
XR_001753634.2:n.1667C>T
XR_935763.1:n.1667C>T