Canonical Allele Identifier: CA376717671

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50679103G>C (hg19) ; chr10:g.49471057G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49471057G>C , CM000672.2:g.49471057G>C	GRCh38
NC_000010.10:g.50679103G>C , CM000672.1:g.50679103G>C	GRCh37
NC_000010.9:g.50349109G>C	NCBI36
NG_009442.1:g.73045C>G , LRG_465:g.73045C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.2988C>G MANE Select	ENSP00000348089.5:p.Phe996Leu
ENST00000679552.1:n.142-168C>G
ENST00000679871.1:n.134C>G
ENST00000679974.1:n.120-168C>G
ENST00000681632.1:n.4391C>G
ENST00000681659.1:c.2829C>G	ENSP00000505631.1:p.Phe943Leu
ENST00000355832.9:c.2988C>G	ENSP00000348089.5:p.Phe996Leu
ENST00000623073.3:c.*1284C>G	ENSP00000485650.1:n.*1284C>G
ENST00000623115.3:c.1098C>G	ENSP00000485321.1:p.Phe366Leu
ENST00000624341.3:c.820C>G
NM_000124.3:c.2988C>G	NP_000115.1:p.Phe996Leu
XR_945953.1:n.243-508G>C
NM_001346440.1:c.2988C>G	NP_001333369.1:p.Phe996Leu
NM_000124.4:c.2988C>G MANE Select	NP_000115.1:p.Phe996Leu
NM_001346440.2:c.2988C>G	NP_001333369.1:p.Phe996Leu