Canonical Allele Identifier: CA694376346

Gene: ERCC5 BIVM-ERCC5

Linked Data

• dbSNP Id: rs1178413551
• MyVariant Identifiers: chr13:g.103525454T>C (hg19) ; chr13:g.102873104T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102873104T>C , CM000675.2:g.102873104T>C	GRCh38
NC_000013.10:g.103525454T>C , CM000675.1:g.103525454T>C	GRCh37
NC_000013.9:g.102323455T>C	NCBI36
NG_007146.1:g.32281T>C , LRG_464:g.32281T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.3826T>C (ERCC5)
ENST00000682869.1:n.3529-155T>C (ERCC5)
ENST00000683246.1:n.4362T>C (ERCC5)
ENST00000683642.1:n.2955T>C (ERCC5)
ENST00000639132.1:c.3555-155T>C (BIVM-ERCC5)	ENSP00000492684.1:n.3555-155T>C
ENST00000639435.1:c.4242-155T>C (BIVM-ERCC5)	ENSP00000491742.1:n.4242-155T>C
ENST00000651002.1:c.*2641-155T>C (ERCC5)	ENSP00000498809.1:n.*2641-155T>C
ENST00000651055.1:n.3009-157T>C (ERCC5)
ENST00000651281.1:n.3248-155T>C (ERCC5)
ENST00000651387.1:n.2364-155T>C (ERCC5)
ENST00000651470.1:c.*52-155T>C (ERCC5)	ENSP00000498701.1:n.*52-155T>C
ENST00000652225.2:c.2880-155T>C (ERCC5) MANE Select	ENSP00000498881.2:n.2880-155T>C
ENST00000652613.1:c.2376-155T>C (ERCC5)	ENSP00000498357.1:n.2376-155T>C
ENST00000355739.8:c.2880-155T>C (ERCC5)	ENSP00000347978.4:n.2880-155T>C
ENST00000375954.1:c.579-155T>C (ERCC5)	ENSP00000365121.1:n.579-155T>C
ENST00000610537.4:c.2877-155T>C (ERCC5)	ENSP00000478667.1:n.2877-155T>C
NM_000123.3:c.2880-155T>C , LRG_464t1:c.2880-155T>C (ERCC5)	NP_000114.2:n.2880-155T>C
NM_001204425.1:c.4242-155T>C (BIVM-ERCC5)	NP_001191354.1:n.4242-155T>C
NM_000123.4:c.2880-155T>C (ERCC5) MANE Select	NP_000114.3:n.2880-155T>C
NM_001204425.2:c.4242-155T>C (BIVM-ERCC5)	NP_001191354.2:n.4242-155T>C