Canonical Allele Identifier: CA2585785516

Gene: ERCC2

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352410_45352427del , CM000681.2:g.45352410_45352427del	GRCh38
NC_000019.9:g.45855668_45855685del , CM000681.1:g.45855668_45855685del	GRCh37
NC_000019.8:g.50547508_50547525del	NCBI36
NG_007067.2:g.23162_23179del , LRG_461:g.23162_23179del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.2047-74_2047-57del	ENSP00000375808.4:n.2047-74_2047-57del
ENST00000682414.1:c.2047-74_2047-57del	ENSP00000507019.1:n.2047-74_2047-57del
ENST00000682508.1:n.2076-74_2076-57del
ENST00000684218.1:c.*1305-74_*1305-57del	ENSP00000507804.1:n.*1305-74_*1305-57del
ENST00000684264.1:n.1603-74_1603-57del
ENST00000684407.1:c.1924-74_1924-57del	ENSP00000507775.1:n.1924-74_1924-57del
ENST00000684458.1:c.*533-74_*533-57del	ENSP00000508260.1:n.*533-74_*533-57del
ENST00000684468.1:n.1759-74_1759-57del
ENST00000391945.10:c.2047-74_2047-57del MANE Select	ENSP00000375809.4:n.2047-74_2047-57del
ENST00000646507.1:n.2144-74_2144-57del
ENST00000391941.6:c.1975-74_1975-57del	ENSP00000375805.2:n.1975-74_1975-57del
ENST00000391942.6:n.1218-74_1218-57del
ENST00000391944.7:c.1813-74_1813-57del	ENSP00000375808.3:n.1813-74_1813-57del
ENST00000391945.8:c.2047-74_2047-57del	ENSP00000375809.3:n.2047-74_2047-57del
ENST00000588652.5:n.2135-74_2135-57del
NM_000400.3:c.2047-74_2047-57del , LRG_461t1:c.2047-74_2047-57del	NP_000391.1:n.2047-74_2047-57del
XM_011526611.1:c.1969-74_1969-57del	XP_011524913.1:n.1969-74_1969-57del
XM_011526611.2:c.1969-74_1969-57del	XP_011524913.1:n.1969-74_1969-57del
XM_017026467.1:c.1924-74_1924-57del	XP_016881956.1:n.1924-74_1924-57del
XR_001753633.2:n.2094-74_2094-57del
XR_001753634.2:n.2030-74_2030-57del
NM_000400.4:c.2047-74_2047-57del MANE Select	NP_000391.1:n.2047-74_2047-57del