Canonical Allele Identifier: CA406360847

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45855471T>G (hg19) ; chr19:g.45352213T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352213T>G , CM000681.2:g.45352213T>G	GRCh38
NC_000019.9:g.45855471T>G , CM000681.1:g.45855471T>G	GRCh37
NC_000019.8:g.50547311T>G	NCBI36
NG_007067.2:g.23375A>C , LRG_461:g.23375A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.2186A>C	ENSP00000375808.4:p.His729Pro
ENST00000682414.1:c.2186A>C	ENSP00000507019.1:p.His729Pro
ENST00000682508.1:n.2215A>C
ENST00000684218.1:c.*1444A>C	ENSP00000507804.1:n.*1444A>C
ENST00000684264.1:n.1742A>C
ENST00000684407.1:c.2063A>C	ENSP00000507775.1:p.His688Pro
ENST00000684458.1:c.*672A>C	ENSP00000508260.1:n.*672A>C
ENST00000684468.1:n.1898A>C
ENST00000391945.10:c.2186A>C MANE Select	ENSP00000375809.4:p.His729Pro
ENST00000646507.1:n.2283A>C
ENST00000391941.6:c.2114A>C	ENSP00000375805.2:p.His705Pro
ENST00000391942.6:n.1357A>C
ENST00000391944.7:c.1952A>C	ENSP00000375808.3:p.His651Pro
ENST00000391945.8:c.2186A>C	ENSP00000375809.3:p.His729Pro
ENST00000588652.5:n.2274A>C
NM_000400.3:c.2186A>C , LRG_461t1:c.2186A>C	NP_000391.1:p.His729Pro
XM_011526611.1:c.2108A>C	XP_011524913.1:p.His703Pro
XM_011526611.2:c.2108A>C	XP_011524913.1:p.His703Pro
XM_017026467.1:c.2063A>C	XP_016881956.1:p.His688Pro
XR_001753633.2:n.2233A>C
XR_001753634.2:n.2169A>C
NM_000400.4:c.2186A>C MANE Select	NP_000391.1:p.His729Pro