Canonical Allele Identifier: CA694376376
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

dbSNP Id: rs1240454318

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102873219_102873222del , CM000675.2:g.102873219_102873222del GRCh38
NC_000013.10:g.103525569_103525572del , CM000675.1:g.103525569_103525572del GRCh37
NC_000013.9:g.102323570_102323573del NCBI36
NG_007146.1:g.32396_32399del , LRG_464:g.32396_32399del

Transcript Alleles

HGVS Amino-acid change
ENST00000682632.1:n.3941_3944del (ERCC5)
ENST00000682869.1:n.3529-40_3529-37del (ERCC5)
ENST00000683246.1:n.4477_4480del (ERCC5)
ENST00000683642.1:n.3070_3073del (ERCC5)
ENST00000639132.1:c.3555-40_3555-37del (BIVM-ERCC5) ENSP00000492684.1:n.3555-40_3555-37del
ENST00000639435.1:c.4242-40_4242-37del (BIVM-ERCC5) ENSP00000491742.1:n.4242-40_4242-37del
ENST00000651002.1:c.*2641-40_*2641-37del (ERCC5) ENSP00000498809.1:n.*2641-40_*2641-37del
ENST00000651055.1:n.3009-42_3009-39del (ERCC5)
ENST00000651281.1:n.3248-40_3248-37del (ERCC5)
ENST00000651387.1:n.2364-40_2364-37del (ERCC5)
ENST00000651470.1:c.*52-40_*52-37del (ERCC5) ENSP00000498701.1:n.*52-40_*52-37del
ENST00000652225.2:c.2880-40_2880-37del (ERCC5) MANE Select ENSP00000498881.2:n.2880-40_2880-37del
ENST00000652613.1:c.2376-40_2376-37del (ERCC5) ENSP00000498357.1:n.2376-40_2376-37del
ENST00000355739.8:c.2880-40_2880-37del (ERCC5) ENSP00000347978.4:n.2880-40_2880-37del
ENST00000375954.1:c.579-40_579-37del (ERCC5) ENSP00000365121.1:n.579-40_579-37del
ENST00000610537.4:c.2877-40_2877-37del (ERCC5) ENSP00000478667.1:n.2877-40_2877-37del
NM_000123.3:c.2880-40_2880-37del , LRG_464t1:c.2880-40_2880-37del (ERCC5) NP_000114.2:n.2880-40_2880-37del
NM_001204425.1:c.4242-40_4242-37del (BIVM-ERCC5) NP_001191354.1:n.4242-40_4242-37del
NM_000123.4:c.2880-40_2880-37del (ERCC5) MANE Select NP_000114.3:n.2880-40_2880-37del
NM_001204425.2:c.4242-40_4242-37del (BIVM-ERCC5) NP_001191354.2:n.4242-40_4242-37del