Canonical Allele Identifier: CA507821958

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45867165T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45363907T>G , CM000681.2:g.45363907T>G	GRCh38
NC_000019.9:g.45867165T>G , CM000681.1:g.45867165T>G	GRCh37
NC_000019.8:g.50559005T>G	NCBI36
NG_007067.2:g.11681A>C , LRG_461:g.11681A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.954A>C	ENSP00000375808.4:p.Ala318=
ENST00000682414.1:c.954A>C	ENSP00000507019.1:p.Ala318=
ENST00000682508.1:n.983A>C
ENST00000684218.1:c.*212A>C	ENSP00000507804.1:n.*212A>C
ENST00000684407.1:c.831A>C	ENSP00000507775.1:p.Ala277=
ENST00000684458.1:c.954A>C	ENSP00000508260.1:p.Ala318=
ENST00000391945.10:c.954A>C MANE Select	ENSP00000375809.4:p.Ala318=
ENST00000587376.6:c.77A>C
ENST00000646507.1:n.1051A>C
ENST00000391941.6:c.882A>C	ENSP00000375805.2:p.Ala294=
ENST00000391944.7:c.720A>C	ENSP00000375808.3:p.Ala240=
ENST00000391945.8:c.954A>C	ENSP00000375809.3:p.Ala318=
ENST00000485403.6:c.882A>C	ENSP00000431229.2:p.Ala294=
ENST00000587376.5:c.77A>C
NM_000400.3:c.954A>C , LRG_461t1:c.954A>C	NP_000391.1:p.Ala318=
NM_001130867.1:c.882A>C	NP_001124339.1:p.Ala294=
XM_011526611.1:c.876A>C	XP_011524913.1:p.Ala292=
XR_935763.1:n.1001A>C
XM_011526611.2:c.876A>C	XP_011524913.1:p.Ala292=
XM_017026467.1:c.831A>C	XP_016881956.1:p.Ala277=
XR_001753633.2:n.1001A>C
XR_001753634.2:n.1001A>C
NM_000400.4:c.954A>C MANE Select	NP_000391.1:p.Ala318=
NM_001130867.2:c.882A>C	NP_001124339.1:p.Ala294=