Canonical Allele Identifier: CA406362328

Gene: ERCC2

Linked Data

• ClinVar Variation Id: 559886
• ClinVar RCV Id: RCV000677677
• dbSNP Id: rs1555775416
• MyVariant Identifiers: chr19:g.45855565G>A (hg19) ; chr19:g.45352307G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352307G>A , CM000681.2:g.45352307G>A	GRCh38
NC_000019.9:g.45855565G>A , CM000681.1:g.45855565G>A	GRCh37
NC_000019.8:g.50547405G>A	NCBI36
NG_007067.2:g.23281C>T , LRG_461:g.23281C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.2092C>T	ENSP00000375808.4:p.Gln698Ter
ENST00000682414.1:c.2092C>T	ENSP00000507019.1:p.Gln698Ter
ENST00000682508.1:n.2121C>T
ENST00000684218.1:c.*1350C>T	ENSP00000507804.1:n.*1350C>T
ENST00000684264.1:n.1648C>T
ENST00000684407.1:c.1969C>T	ENSP00000507775.1:p.Gln657Ter
ENST00000684458.1:c.*578C>T	ENSP00000508260.1:n.*578C>T
ENST00000684468.1:n.1804C>T
ENST00000391945.10:c.2092C>T MANE Select	ENSP00000375809.4:p.Gln698Ter
ENST00000646507.1:n.2189C>T
ENST00000391941.6:c.2020C>T	ENSP00000375805.2:p.Gln674Ter
ENST00000391942.6:n.1263C>T
ENST00000391944.7:c.1858C>T	ENSP00000375808.3:p.Gln620Ter
ENST00000391945.8:c.2092C>T	ENSP00000375809.3:p.Gln698Ter
ENST00000588652.5:n.2180C>T
NM_000400.3:c.2092C>T , LRG_461t1:c.2092C>T	NP_000391.1:p.Gln698Ter
XM_011526611.1:c.2014C>T	XP_011524913.1:p.Gln672Ter
XM_011526611.2:c.2014C>T	XP_011524913.1:p.Gln672Ter
XM_017026467.1:c.1969C>T	XP_016881956.1:p.Gln657Ter
XR_001753633.2:n.2139C>T
XR_001753634.2:n.2075C>T
NM_000400.4:c.2092C>T MANE Select	NP_000391.1:p.Gln698Ter