Canonical Allele Identifier: CA2800409750
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102873119_102873122del , CM000675.2:g.102873119_102873122del GRCh38
NC_000013.10:g.103525469_103525472del , CM000675.1:g.103525469_103525472del GRCh37
NC_000013.9:g.102323470_102323473del NCBI36
NG_007146.1:g.32296_32299del , LRG_464:g.32296_32299del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.3841_3844del (ERCC5)
ENST00000682869.1:n.3529-140_3529-137del (ERCC5)
ENST00000683246.1:n.4377_4380del (ERCC5)
ENST00000683642.1:n.2970_2973del (ERCC5)
ENST00000639132.1:c.3555-140_3555-137del (BIVM-ERCC5) ENSP00000492684.1:n.3555-140_3555-137del
ENST00000639435.1:c.4242-140_4242-137del (BIVM-ERCC5) ENSP00000491742.1:n.4242-140_4242-137del
ENST00000651002.1:c.*2641-140_*2641-137del (ERCC5) ENSP00000498809.1:n.*2641-140_*2641-137del
ENST00000651055.1:n.3009-142_3009-139del (ERCC5)
ENST00000651281.1:n.3248-140_3248-137del (ERCC5)
ENST00000651387.1:n.2364-140_2364-137del (ERCC5)
ENST00000651470.1:c.*52-140_*52-137del (ERCC5) ENSP00000498701.1:n.*52-140_*52-137del
ENST00000652225.2:c.2880-140_2880-137del (ERCC5) MANE Select ENSP00000498881.2:n.2880-140_2880-137del
ENST00000652613.1:c.2376-140_2376-137del (ERCC5) ENSP00000498357.1:n.2376-140_2376-137del
ENST00000355739.8:c.2880-140_2880-137del (ERCC5) ENSP00000347978.4:n.2880-140_2880-137del
ENST00000375954.1:c.579-140_579-137del (ERCC5) ENSP00000365121.1:n.579-140_579-137del
ENST00000610537.4:c.2877-140_2877-137del (ERCC5) ENSP00000478667.1:n.2877-140_2877-137del
NM_000123.3:c.2880-140_2880-137del , LRG_464t1:c.2880-140_2880-137del (ERCC5) NP_000114.2:n.2880-140_2880-137del
NM_001204425.1:c.4242-140_4242-137del (BIVM-ERCC5) NP_001191354.1:n.4242-140_4242-137del
NM_000123.4:c.2880-140_2880-137del (ERCC5) MANE Select NP_000114.3:n.2880-140_2880-137del
NM_001204425.2:c.4242-140_4242-137del (BIVM-ERCC5) NP_001191354.2:n.4242-140_4242-137del