Canonical Allele Identifier: CA376717199

Gene: ERCC6

Linked Data

• dbSNP Id: rs1225942149
• gnomAD v4: 10-49470886-G-A
• MyVariant Identifiers: chr10:g.50678932G>A (hg19) ; chr10:g.49470886G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470886G>A , CM000672.2:g.49470886G>A	GRCh38
NC_000010.10:g.50678932G>A , CM000672.1:g.50678932G>A	GRCh37
NC_000010.9:g.50348938G>A	NCBI36
NG_009442.1:g.73216C>T , LRG_465:g.73216C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3074C>T MANE Select	ENSP00000348089.5:p.Thr1025Ile
ENST00000679552.1:n.145C>T
ENST00000679871.1:n.220C>T
ENST00000679974.1:n.123C>T
ENST00000681632.1:n.4477C>T
ENST00000681659.1:c.2915C>T	ENSP00000505631.1:p.Thr972Ile
ENST00000355832.9:c.3074C>T	ENSP00000348089.5:p.Thr1025Ile
ENST00000623073.3:c.*1370C>T	ENSP00000485650.1:n.*1370C>T
ENST00000623115.3:c.1184C>T	ENSP00000485321.1:p.Thr395Ile
ENST00000624341.3:c.906C>T
NM_000124.3:c.3074C>T	NP_000115.1:p.Thr1025Ile
XR_945953.1:n.243-679G>A
NM_001346440.1:c.3074C>T	NP_001333369.1:p.Thr1025Ile
NM_000124.4:c.3074C>T MANE Select	NP_000115.1:p.Thr1025Ile
NM_001346440.2:c.3074C>T	NP_001333369.1:p.Thr1025Ile