Canonical Allele Identifier: CA406373089

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45867151A>C (hg19) ; chr19:g.45363893A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45363893A>C , CM000681.2:g.45363893A>C	GRCh38
NC_000019.9:g.45867151A>C , CM000681.1:g.45867151A>C	GRCh37
NC_000019.8:g.50558991A>C	NCBI36
NG_007067.2:g.11695T>G , LRG_461:g.11695T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.968T>G	ENSP00000375808.4:p.Ile323Ser
ENST00000682414.1:c.968T>G	ENSP00000507019.1:p.Ile323Ser
ENST00000682508.1:n.997T>G
ENST00000684218.1:c.*226T>G	ENSP00000507804.1:n.*226T>G
ENST00000684407.1:c.845T>G	ENSP00000507775.1:p.Ile282Ser
ENST00000684458.1:c.968T>G	ENSP00000508260.1:p.Ile323Ser
ENST00000391945.10:c.968T>G MANE Select	ENSP00000375809.4:p.Ile323Ser
ENST00000587376.6:c.91T>G
ENST00000646507.1:n.1065T>G
ENST00000391941.6:c.896T>G	ENSP00000375805.2:p.Ile299Ser
ENST00000391944.7:c.734T>G	ENSP00000375808.3:p.Ile245Ser
ENST00000391945.8:c.968T>G	ENSP00000375809.3:p.Ile323Ser
ENST00000485403.6:c.896T>G	ENSP00000431229.2:p.Ile299Ser
ENST00000587376.5:c.91T>G
NM_000400.3:c.968T>G , LRG_461t1:c.968T>G	NP_000391.1:p.Ile323Ser
NM_001130867.1:c.896T>G	NP_001124339.1:p.Ile299Ser
XM_011526611.1:c.890T>G	XP_011524913.1:p.Ile297Ser
XR_935763.1:n.1015T>G
XM_011526611.2:c.890T>G	XP_011524913.1:p.Ile297Ser
XM_017026467.1:c.845T>G	XP_016881956.1:p.Ile282Ser
XR_001753633.2:n.1015T>G
XR_001753634.2:n.1015T>G
NM_000400.4:c.968T>G MANE Select	NP_000391.1:p.Ile323Ser
NM_001130867.2:c.896T>G	NP_001124339.1:p.Ile299Ser