Canonical Allele Identifier: CA376714948

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50678581G>T (hg19) ; chr10:g.49470535G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470535G>T , CM000672.2:g.49470535G>T	GRCh38
NC_000010.10:g.50678581G>T , CM000672.1:g.50678581G>T	GRCh37
NC_000010.9:g.50348587G>T	NCBI36
NG_009442.1:g.73567C>A , LRG_465:g.73567C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3425C>A MANE Select	ENSP00000348089.5:p.Ser1142Tyr
ENST00000679552.1:n.496C>A
ENST00000679871.1:n.571C>A
ENST00000679974.1:n.474C>A
ENST00000681632.1:n.4828C>A
ENST00000681659.1:c.3266C>A	ENSP00000505631.1:p.Ser1089Tyr
ENST00000355832.9:c.3425C>A	ENSP00000348089.5:p.Ser1142Tyr
ENST00000623073.3:c.*1721C>A	ENSP00000485650.1:n.*1721C>A
ENST00000623115.3:c.1535C>A	ENSP00000485321.1:p.Ser512Tyr
ENST00000624341.3:c.1257C>A
NM_000124.3:c.3425C>A	NP_000115.1:p.Ser1142Tyr
XR_945953.1:n.243-1030G>T
NM_001346440.1:c.3425C>A	NP_001333369.1:p.Ser1142Tyr
NM_000124.4:c.3425C>A MANE Select	NP_000115.1:p.Ser1142Tyr
NM_001346440.2:c.3425C>A	NP_001333369.1:p.Ser1142Tyr