Canonical Allele Identifier: CA2115203198
Gene: BIVM-ERCC5 HGNC NCBI
ERCC5 HGNC NCBI

Linked Data

dbSNP Id: rs1881935625

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102845897T>G , CM000675.2:g.102845897T>G GRCh38
NC_000013.10:g.103498247T>G , CM000675.1:g.103498247T>G GRCh37
NC_000013.9:g.102296248T>G NCBI36
NG_007146.1:g.5074T>G , LRG_464:g.5074T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000638434.1:c.363-7860T>G (BIVM-ERCC5)
ENST00000639118.1:c.363-3221T>G (BIVM-ERCC5)
ENST00000639132.1:c.763+6094T>G (BIVM-ERCC5) ENSP00000492684.1:n.763+6094T>G
ENST00000639435.1:c.1450+6094T>G (BIVM-ERCC5) ENSP00000491742.1:n.1450+6094T>G
ENST00000651002.1:c.-370T>G (ERCC5) ENSP00000498809.1:n.-370T>G
ENST00000652613.1:c.-867T>G (ERCC5) ENSP00000498357.1:n.-867T>G
ENST00000355739.8:c.-370T>G (ERCC5) ENSP00000347978.4:n.-370T>G
ENST00000535557.5:c.-370T>G (ERCC5) ENSP00000442117.1:n.-370T>G
ENST00000602836.1:c.1364+6094T>G (BIVM-ERCC5)
NM_000123.3:c.-370T>G , LRG_464t1:c.-370T>G (ERCC5) NP_000114.2:n.-370T>G
NM_001204425.1:c.1450+6094T>G (BIVM-ERCC5) NP_001191354.1:n.1450+6094T>G
NM_001204425.2:c.1450+6094T>G (BIVM-ERCC5) NP_001191354.2:n.1450+6094T>G