Canonical Allele Identifier: CA406363928

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45856065T>G (hg19) ; chr19:g.45352807T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352807T>G , CM000681.2:g.45352807T>G	GRCh38
NC_000019.9:g.45856065T>G , CM000681.1:g.45856065T>G	GRCh37
NC_000019.8:g.50547905T>G	NCBI36
NG_007067.2:g.22781A>C , LRG_461:g.22781A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1841A>C	ENSP00000375808.4:p.Tyr614Ser
ENST00000682414.1:c.1841A>C	ENSP00000507019.1:p.Tyr614Ser
ENST00000682508.1:n.1870A>C
ENST00000684218.1:c.*1099A>C	ENSP00000507804.1:n.*1099A>C
ENST00000684264.1:n.1397A>C
ENST00000684407.1:c.1718A>C	ENSP00000507775.1:p.Tyr573Ser
ENST00000684458.1:c.*327A>C	ENSP00000508260.1:n.*327A>C
ENST00000684468.1:n.1553A>C
ENST00000391945.10:c.1841A>C MANE Select	ENSP00000375809.4:p.Tyr614Ser
ENST00000646507.1:n.1938A>C
ENST00000391941.6:c.1769A>C	ENSP00000375805.2:p.Tyr590Ser
ENST00000391942.6:n.1012A>C
ENST00000391944.7:c.1607A>C	ENSP00000375808.3:p.Tyr536Ser
ENST00000391945.8:c.1841A>C	ENSP00000375809.3:p.Tyr614Ser
ENST00000588652.5:n.1929A>C
NM_000400.3:c.1841A>C , LRG_461t1:c.1841A>C	NP_000391.1:p.Tyr614Ser
XM_011526611.1:c.1763A>C	XP_011524913.1:p.Tyr588Ser
XM_011526611.2:c.1763A>C	XP_011524913.1:p.Tyr588Ser
XM_017026467.1:c.1718A>C	XP_016881956.1:p.Tyr573Ser
XR_001753633.2:n.1888A>C
XR_001753634.2:n.1824A>C
NM_000400.4:c.1841A>C MANE Select	NP_000391.1:p.Tyr614Ser