Canonical Allele Identifier: CA376755240

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50732751G>A (hg19) ; chr10:g.49524705G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49524705G>A , CM000672.2:g.49524705G>A	GRCh38
NC_000010.10:g.50732751G>A , CM000672.1:g.50732751G>A	GRCh37
NC_000010.9:g.50402757G>A	NCBI36
NG_009442.1:g.19397C>T , LRG_465:g.19397C>T
NG_033155.1:g.4577C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.725C>T MANE Select	ENSP00000348089.5:p.Thr242Ile
ENST00000447839.7:c.725C>T MANE Plus Clinical	ENSP00000387966.2:p.Thr242Ile
ENST00000679596.1:c.*354C>T	ENSP00000504862.1:n.*354C>T
ENST00000679811.1:n.808C>T
ENST00000680107.1:c.652+3712C>T	ENSP00000505909.1:n.652+3712C>T
ENST00000680233.1:n.818C>T
ENST00000681632.1:n.803C>T
ENST00000681659.1:c.725C>T	ENSP00000505631.1:p.Thr242Ile
ENST00000355832.9:c.725C>T	ENSP00000348089.5:p.Thr242Ile
ENST00000447839.6:c.725C>T	ENSP00000387966.2:p.Thr242Ile
ENST00000515869.1:c.725C>T	ENSP00000423550.1:p.Thr242Ile
NM_000124.3:c.725C>T	NP_000115.1:p.Thr242Ile
NM_001277058.1:c.725C>T	NP_001263987.1:p.Thr242Ile
NM_001277059.1:c.725C>T	NP_001263988.1:p.Thr242Ile
NM_001346440.1:c.725C>T	NP_001333369.1:p.Thr242Ile
NM_000124.4:c.725C>T MANE Select	NP_000115.1:p.Thr242Ile
NM_001277058.2:c.725C>T MANE Plus Clinical	NP_001263987.1:p.Thr242Ile
NM_001277059.2:c.725C>T	NP_001263988.1:p.Thr242Ile
NM_001346440.2:c.725C>T	NP_001333369.1:p.Thr242Ile