Canonical Allele Identifier: CA376716916

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50678882G>T (hg19) ; chr10:g.49470836G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470836G>T , CM000672.2:g.49470836G>T	GRCh38
NC_000010.10:g.50678882G>T , CM000672.1:g.50678882G>T	GRCh37
NC_000010.9:g.50348888G>T	NCBI36
NG_009442.1:g.73266C>A , LRG_465:g.73266C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3124C>A MANE Select	ENSP00000348089.5:p.Pro1042Thr
ENST00000679552.1:n.195C>A
ENST00000679871.1:n.270C>A
ENST00000679974.1:n.173C>A
ENST00000681632.1:n.4527C>A
ENST00000681659.1:c.2965C>A	ENSP00000505631.1:p.Pro989Thr
ENST00000355832.9:c.3124C>A	ENSP00000348089.5:p.Pro1042Thr
ENST00000623073.3:c.*1420C>A	ENSP00000485650.1:n.*1420C>A
ENST00000623115.3:c.1234C>A	ENSP00000485321.1:p.Pro412Thr
ENST00000624341.3:c.956C>A
NM_000124.3:c.3124C>A	NP_000115.1:p.Pro1042Thr
XR_945953.1:n.243-729G>T
NM_001346440.1:c.3124C>A	NP_001333369.1:p.Pro1042Thr
NM_000124.4:c.3124C>A MANE Select	NP_000115.1:p.Pro1042Thr
NM_001346440.2:c.3124C>A	NP_001333369.1:p.Pro1042Thr