Canonical Allele Identifier: CA2576816129

Gene: ERCC2

Linked Data

• gnomAD v4: 19-45352867-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352867G>T , CM000681.2:g.45352867G>T	GRCh38
NC_000019.9:g.45856125G>T , CM000681.1:g.45856125G>T	GRCh37
NC_000019.8:g.50547965G>T	NCBI36
NG_007067.2:g.22721C>A , LRG_461:g.22721C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1832-51C>A	ENSP00000375808.4:n.1832-51C>A
ENST00000682414.1:c.1832-51C>A	ENSP00000507019.1:n.1832-51C>A
ENST00000682508.1:n.1861-51C>A
ENST00000684218.1:c.*1090-51C>A	ENSP00000507804.1:n.*1090-51C>A
ENST00000684264.1:n.1388-51C>A
ENST00000684407.1:c.1709-51C>A	ENSP00000507775.1:n.1709-51C>A
ENST00000684458.1:c.*318-51C>A	ENSP00000508260.1:n.*318-51C>A
ENST00000684468.1:n.1544-51C>A
ENST00000391945.10:c.1832-51C>A MANE Select	ENSP00000375809.4:n.1832-51C>A
ENST00000646507.1:n.1929-51C>A
ENST00000391941.6:c.1760-51C>A	ENSP00000375805.2:n.1760-51C>A
ENST00000391942.6:n.1003-51C>A
ENST00000391944.7:c.1598-51C>A	ENSP00000375808.3:n.1598-51C>A
ENST00000391945.8:c.1832-51C>A	ENSP00000375809.3:n.1832-51C>A
ENST00000588652.5:n.1920-51C>A
NM_000400.3:c.1832-51C>A , LRG_461t1:c.1832-51C>A	NP_000391.1:n.1832-51C>A
XM_011526611.1:c.1754-51C>A	XP_011524913.1:n.1754-51C>A
XM_011526611.2:c.1754-51C>A	XP_011524913.1:n.1754-51C>A
XM_017026467.1:c.1709-51C>A	XP_016881956.1:n.1709-51C>A
XR_001753633.2:n.1879-51C>A
XR_001753634.2:n.1815-51C>A
NM_000400.4:c.1832-51C>A MANE Select	NP_000391.1:n.1832-51C>A