Canonical Allele Identifier: CA376717633

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50679095T>G (hg19) ; chr10:g.49471049T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49471049T>G , CM000672.2:g.49471049T>G	GRCh38
NC_000010.10:g.50679095T>G , CM000672.1:g.50679095T>G	GRCh37
NC_000010.9:g.50349101T>G	NCBI36
NG_009442.1:g.73053A>C , LRG_465:g.73053A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.2996A>C MANE Select	ENSP00000348089.5:p.Asn999Thr
ENST00000679552.1:n.142-160A>C
ENST00000679871.1:n.142A>C
ENST00000679974.1:n.120-160A>C
ENST00000681632.1:n.4399A>C
ENST00000681659.1:c.2837A>C	ENSP00000505631.1:p.Asn946Thr
ENST00000355832.9:c.2996A>C	ENSP00000348089.5:p.Asn999Thr
ENST00000623073.3:c.*1292A>C	ENSP00000485650.1:n.*1292A>C
ENST00000623115.3:c.1106A>C	ENSP00000485321.1:p.Asn369Thr
ENST00000624341.3:c.828A>C
NM_000124.3:c.2996A>C	NP_000115.1:p.Asn999Thr
XR_945953.1:n.243-516T>G
NM_001346440.1:c.2996A>C	NP_001333369.1:p.Asn999Thr
NM_000124.4:c.2996A>C MANE Select	NP_000115.1:p.Asn999Thr
NM_001346440.2:c.2996A>C	NP_001333369.1:p.Asn999Thr