Canonical Allele Identifier: CA376718762

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50680518T>A (hg19) ; chr10:g.49472472T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49472472T>A , CM000672.2:g.49472472T>A	GRCh38
NC_000010.10:g.50680518T>A , CM000672.1:g.50680518T>A	GRCh37
NC_000010.9:g.50350524T>A	NCBI36
NG_009442.1:g.71630A>T , LRG_465:g.71630A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.2830-2A>T MANE Select	ENSP00000348089.5:n.2830-2A>T
ENST00000681632.1:n.4231A>T
ENST00000681659.1:c.2671-2A>T	ENSP00000505631.1:n.2671-2A>T
ENST00000355832.9:c.2830-2A>T	ENSP00000348089.5:n.2830-2A>T
ENST00000623073.3:c.*1126-2A>T	ENSP00000485650.1:n.*1126-2A>T
ENST00000623115.3:c.940-2A>T	ENSP00000485321.1:n.940-2A>T
ENST00000624341.3:c.662-2A>T
NM_000124.3:c.2830-2A>T	NP_000115.1:n.2830-2A>T
XR_945953.1:n.690-231T>A
NM_001346440.1:c.2830-2A>T	NP_001333369.1:n.2830-2A>T
NM_000124.4:c.2830-2A>T MANE Select	NP_000115.1:n.2830-2A>T
NM_001346440.2:c.2830-2A>T	NP_001333369.1:n.2830-2A>T