Canonical Allele Identifier: CA2623613074
Gene: BIVM-ERCC5 HGNC NCBI
ERCC5 HGNC NCBI

Linked Data

gnomAD v4: 13-102845856-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102845856G>T , CM000675.2:g.102845856G>T GRCh38
NC_000013.10:g.103498206G>T , CM000675.1:g.103498206G>T GRCh37
NC_000013.9:g.102296207G>T NCBI36
NG_007146.1:g.5033G>T , LRG_464:g.5033G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000638434.1:c.363-7901G>T (BIVM-ERCC5)
ENST00000639118.1:c.363-3262G>T (BIVM-ERCC5)
ENST00000639132.1:c.763+6053G>T (BIVM-ERCC5) ENSP00000492684.1:n.763+6053G>T
ENST00000639435.1:c.1450+6053G>T (BIVM-ERCC5) ENSP00000491742.1:n.1450+6053G>T
ENST00000651002.1:c.-411G>T (ERCC5) ENSP00000498809.1:n.-411G>T
ENST00000355739.8:c.-411G>T (ERCC5) ENSP00000347978.4:n.-411G>T
ENST00000535557.5:c.-411G>T (ERCC5) ENSP00000442117.1:n.-411G>T
ENST00000602836.1:c.1364+6053G>T (BIVM-ERCC5)
NM_000123.3:c.-411G>T , LRG_464t1:c.-411G>T (ERCC5) NP_000114.2:n.-411G>T
NM_001204425.1:c.1450+6053G>T (BIVM-ERCC5) NP_001191354.1:n.1450+6053G>T
NM_001204425.2:c.1450+6053G>T (BIVM-ERCC5) NP_001191354.2:n.1450+6053G>T
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