Canonical Allele Identifier: CA376717849

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50679141T>G (hg19) ; chr10:g.49471095T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49471095T>G , CM000672.2:g.49471095T>G	GRCh38
NC_000010.10:g.50679141T>G , CM000672.1:g.50679141T>G	GRCh37
NC_000010.9:g.50349147T>G	NCBI36
NG_009442.1:g.73007A>C , LRG_465:g.73007A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.2950A>C MANE Select	ENSP00000348089.5:p.Asn984His
ENST00000679552.1:n.142-206A>C
ENST00000679871.1:n.96A>C
ENST00000679974.1:n.120-206A>C
ENST00000681632.1:n.4353A>C
ENST00000681659.1:c.2791A>C	ENSP00000505631.1:p.Asn931His
ENST00000355832.9:c.2950A>C	ENSP00000348089.5:p.Asn984His
ENST00000623073.3:c.*1246A>C	ENSP00000485650.1:n.*1246A>C
ENST00000623115.3:c.1060A>C	ENSP00000485321.1:p.Asn354His
ENST00000624341.3:c.782A>C
NM_000124.3:c.2950A>C	NP_000115.1:p.Asn984His
XR_945953.1:n.243-470T>G
NM_001346440.1:c.2950A>C	NP_001333369.1:p.Asn984His
NM_000124.4:c.2950A>C MANE Select	NP_000115.1:p.Asn984His
NM_001346440.2:c.2950A>C	NP_001333369.1:p.Asn984His