Canonical Allele Identifier: CA406379637

Gene: ERCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45369132C>A , CM000681.2:g.45369132C>A	GRCh38
NC_000019.9:g.45872390C>A , CM000681.1:g.45872390C>A	GRCh37
NC_000019.8:g.50564230C>A	NCBI36
NG_007067.2:g.6456G>T , LRG_461:g.6456G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000400.4:c.121G>T MANE Select	NP_000391.1:p.Glu41Ter
ENST00000391945.10:c.121G>T MANE Select	ENSP00000375809.4:p.Glu41Ter
NM_000400.3:c.121G>T , LRG_461t1:c.121G>T	NP_000391.1:p.Glu41Ter
NM_001130867.1:c.49G>T	NP_001124339.1:p.Glu17Ter
NM_001130867.2:c.49G>T	NP_001124339.1:p.Glu17Ter
ENST00000391941.6:c.49G>T	ENSP00000375805.2:p.Glu17Ter
ENST00000391944.7:c.121G>T	ENSP00000375808.3:p.Glu41Ter
ENST00000391944.8:c.121G>T	ENSP00000375808.4:p.Glu41Ter
ENST00000391945.8:c.121G>T	ENSP00000375809.3:p.Glu41Ter
ENST00000485403.6:c.49G>T	ENSP00000431229.2:p.Glu17Ter
ENST00000586131.5:c.49G>T	ENSP00000464887.1:p.Glu17Ter
ENST00000586131.6:c.49G>T	ENSP00000464887.1:p.Glu17Ter
ENST00000586441.1:n.36G>T
ENST00000586737.5:n.36G>T
ENST00000586856.1:c.34-140G>T	ENSP00000466998.1:n.34-140G>T
ENST00000591309.5:c.121G>T	ENSP00000465207.1:p.Glu41Ter
ENST00000646507.1:n.141G>T
ENST00000682414.1:c.121G>T	ENSP00000507019.1:p.Glu41Ter
ENST00000682508.1:n.73G>T
ENST00000684218.1:c.121G>T	ENSP00000507804.1:p.Glu41Ter
ENST00000684407.1:c.-3G>T	ENSP00000507775.1:n.-3G>T
ENST00000684458.1:c.121G>T	ENSP00000508260.1:p.Glu41Ter
XM_011526611.1:c.106-140G>T	XP_011524913.1:n.106-140G>T
XM_011526611.2:c.106-140G>T	XP_011524913.1:n.106-140G>T
XM_017026467.1:c.-3G>T	XP_016881956.1:n.-3G>T
XR_001753633.2:n.168G>T
XR_001753634.2:n.168G>T
XR_935763.1:n.168G>T