Canonical Allele Identifier: CA376713476

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50678407A>G (hg19) ; chr10:g.49470361A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470361A>G , CM000672.2:g.49470361A>G	GRCh38
NC_000010.10:g.50678407A>G , CM000672.1:g.50678407A>G	GRCh37
NC_000010.9:g.50348413A>G	NCBI36
NG_009442.1:g.73741T>C , LRG_465:g.73741T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3599T>C MANE Select	ENSP00000348089.5:p.Leu1200Pro
ENST00000679552.1:n.670T>C
ENST00000679871.1:n.745T>C
ENST00000679974.1:n.648T>C
ENST00000681632.1:n.5002T>C
ENST00000681659.1:c.3440T>C	ENSP00000505631.1:p.Leu1147Pro
ENST00000355832.9:c.3599T>C	ENSP00000348089.5:p.Leu1200Pro
ENST00000623073.3:c.*1895T>C	ENSP00000485650.1:n.*1895T>C
ENST00000623115.3:c.1709T>C	ENSP00000485321.1:p.Leu570Pro
ENST00000624341.3:c.1431T>C
NM_000124.3:c.3599T>C	NP_000115.1:p.Leu1200Pro
XR_945953.1:n.243-1204A>G
NM_001346440.1:c.3599T>C	NP_001333369.1:p.Leu1200Pro
NM_000124.4:c.3599T>C MANE Select	NP_000115.1:p.Leu1200Pro
NM_001346440.2:c.3599T>C	NP_001333369.1:p.Leu1200Pro