Canonical Allele Identifier: CA484859225

Gene: ERCC5 BIVM-ERCC5

Linked Data

• MyVariant Identifiers: chr13:g.103525666T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102873316T>C , CM000675.2:g.102873316T>C	GRCh38
NC_000013.10:g.103525666T>C , CM000675.1:g.103525666T>C	GRCh37
NC_000013.9:g.102323667T>C	NCBI36
NG_007146.1:g.32493T>C , LRG_464:g.32493T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.4038T>C (ERCC5)
ENST00000682869.1:n.3586T>C (ERCC5)
ENST00000683246.1:n.4574T>C (ERCC5)
ENST00000683642.1:n.3167T>C (ERCC5)
ENST00000639132.1:c.3612T>C (BIVM-ERCC5)	ENSP00000492684.1:p.Pro1204=
ENST00000639435.1:c.4299T>C (BIVM-ERCC5)	ENSP00000491742.1:p.Pro1433=
ENST00000651002.1:c.*2698T>C (ERCC5)	ENSP00000498809.1:n.*2698T>C
ENST00000651055.1:n.3064T>C (ERCC5)
ENST00000651281.1:n.3305T>C (ERCC5)
ENST00000651387.1:n.2421T>C (ERCC5)
ENST00000651470.1:c.*109T>C (ERCC5)	ENSP00000498701.1:n.*109T>C
ENST00000652225.2:c.2937T>C (ERCC5) MANE Select	ENSP00000498881.2:p.Pro979=
ENST00000652613.1:c.2433T>C (ERCC5)	ENSP00000498357.1:p.Pro811=
ENST00000355739.8:c.2937T>C (ERCC5)	ENSP00000347978.4:p.Pro979=
ENST00000375954.1:c.636T>C (ERCC5)	ENSP00000365121.1:p.Pro212=
ENST00000610537.4:c.2934T>C (ERCC5)	ENSP00000478667.1:p.Pro978=
NM_000123.3:c.2937T>C , LRG_464t1:c.2937T>C (ERCC5)	NP_000114.2:p.Pro979=
NM_001204425.1:c.4299T>C (BIVM-ERCC5)	NP_001191354.1:p.Pro1433=
NM_000123.4:c.2937T>C (ERCC5) MANE Select	NP_000114.3:p.Pro979=
NM_001204425.2:c.4299T>C (BIVM-ERCC5)	NP_001191354.2:p.Pro1433=