Canonical Allele Identifier: CA9512861

Gene: ERCC2

Linked Data

• dbSNP Id: rs754313108
• ExAC: 19:45855490 G / A
• gnomAD v2: 19-45855490-G-A
• gnomAD v3: 19-45352232-G-A
• gnomAD v4: 19-45352232-G-A
• MyVariant Identifiers: chr19:g.45855490G>A (hg19) ; chr19:g.45352232G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352232G>A , CM000681.2:g.45352232G>A	GRCh38
NC_000019.9:g.45855490G>A , CM000681.1:g.45855490G>A	GRCh37
NC_000019.8:g.50547330G>A	NCBI36
NG_007067.2:g.23356C>T , LRG_461:g.23356C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.2167C>T	ENSP00000375808.4:p.Gln723Ter
ENST00000682414.1:c.2167C>T	ENSP00000507019.1:p.Gln723Ter
ENST00000682508.1:n.2196C>T
ENST00000684218.1:c.*1425C>T	ENSP00000507804.1:n.*1425C>T
ENST00000684264.1:n.1723C>T
ENST00000684407.1:c.2044C>T	ENSP00000507775.1:p.Gln682Ter
ENST00000684458.1:c.*653C>T	ENSP00000508260.1:n.*653C>T
ENST00000684468.1:n.1879C>T
ENST00000391945.10:c.2167C>T MANE Select	ENSP00000375809.4:p.Gln723Ter
ENST00000646507.1:n.2264C>T
ENST00000391941.6:c.2095C>T	ENSP00000375805.2:p.Gln699Ter
ENST00000391942.6:n.1338C>T
ENST00000391944.7:c.1933C>T	ENSP00000375808.3:p.Gln645Ter
ENST00000391945.8:c.2167C>T	ENSP00000375809.3:p.Gln723Ter
ENST00000588652.5:n.2255C>T
NM_000400.3:c.2167C>T , LRG_461t1:c.2167C>T	NP_000391.1:p.Gln723Ter
XM_011526611.1:c.2089C>T	XP_011524913.1:p.Gln697Ter
XM_011526611.2:c.2089C>T	XP_011524913.1:p.Gln697Ter
XM_017026467.1:c.2044C>T	XP_016881956.1:p.Gln682Ter
XR_001753633.2:n.2214C>T
XR_001753634.2:n.2150C>T
NM_000400.4:c.2167C>T MANE Select	NP_000391.1:p.Gln723Ter