Canonical Allele Identifier: CA388674990

Gene: ERCC5 BIVM-ERCC5

Linked Data

• MyVariant Identifiers: chr13:g.103527951T>C (hg19) ; chr13:g.102875601T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102875601T>C , CM000675.2:g.102875601T>C	GRCh38
NC_000013.10:g.103527951T>C , CM000675.1:g.103527951T>C	GRCh37
NC_000013.9:g.102325952T>C	NCBI36
NG_007146.1:g.34778T>C , LRG_464:g.34778T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.4360T>C (ERCC5)
ENST00000682869.1:n.3908T>C (ERCC5)
ENST00000683246.1:n.4896T>C (ERCC5)
ENST00000683642.1:n.3489T>C (ERCC5)
ENST00000639132.1:c.3934T>C (BIVM-ERCC5)	ENSP00000492684.1:p.Phe1312Leu
ENST00000639435.1:c.4621T>C (BIVM-ERCC5)	ENSP00000491742.1:p.Phe1541Leu
ENST00000651002.1:c.*3020T>C (ERCC5)	ENSP00000498809.1:n.*3020T>C
ENST00000651055.1:n.3386T>C (ERCC5)
ENST00000651281.1:n.3627T>C (ERCC5)
ENST00000651387.1:n.2743T>C (ERCC5)
ENST00000651470.1:c.*431T>C (ERCC5)	ENSP00000498701.1:n.*431T>C
ENST00000652225.2:c.3259T>C (ERCC5) MANE Select	ENSP00000498881.2:p.Phe1087Leu
ENST00000652613.1:c.2755T>C (ERCC5)	ENSP00000498357.1:p.Phe919Leu
ENST00000355739.8:c.3259T>C (ERCC5)	ENSP00000347978.4:p.Phe1087Leu
ENST00000375954.1:c.958T>C (ERCC5)	ENSP00000365121.1:p.Phe320Leu
ENST00000472247.1:n.419T>C (ERCC5)
ENST00000610537.4:c.3256T>C (ERCC5)	ENSP00000478667.1:p.Phe1086Leu
NM_000123.3:c.3259T>C , LRG_464t1:c.3259T>C (ERCC5)	NP_000114.2:p.Phe1087Leu
NM_001204425.1:c.4621T>C (BIVM-ERCC5)	NP_001191354.1:p.Phe1541Leu
NM_000123.4:c.3259T>C (ERCC5) MANE Select	NP_000114.3:p.Phe1087Leu
NM_001204425.2:c.4621T>C (BIVM-ERCC5)	NP_001191354.2:p.Phe1541Leu