Canonical Allele Identifier: CA376716339

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50678790T>A (hg19) ; chr10:g.49470744T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470744T>A , CM000672.2:g.49470744T>A	GRCh38
NC_000010.10:g.50678790T>A , CM000672.1:g.50678790T>A	GRCh37
NC_000010.9:g.50348796T>A	NCBI36
NG_009442.1:g.73358A>T , LRG_465:g.73358A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3216A>T MANE Select	ENSP00000348089.5:p.Lys1072Asn
ENST00000679552.1:n.287A>T
ENST00000679871.1:n.362A>T
ENST00000679974.1:n.265A>T
ENST00000681632.1:n.4619A>T
ENST00000681659.1:c.3057A>T	ENSP00000505631.1:p.Lys1019Asn
ENST00000355832.9:c.3216A>T	ENSP00000348089.5:p.Lys1072Asn
ENST00000623073.3:c.*1512A>T	ENSP00000485650.1:n.*1512A>T
ENST00000623115.3:c.1326A>T	ENSP00000485321.1:p.Lys442Asn
ENST00000624341.3:c.1048A>T
NM_000124.3:c.3216A>T	NP_000115.1:p.Lys1072Asn
XR_945953.1:n.243-821T>A
NM_001346440.1:c.3216A>T	NP_001333369.1:p.Lys1072Asn
NM_000124.4:c.3216A>T MANE Select	NP_000115.1:p.Lys1072Asn
NM_001346440.2:c.3216A>T	NP_001333369.1:p.Lys1072Asn