Canonical Allele Identifier: CA376708515

Gene: ERCC6

Linked Data

• COSMIC: COSM1187941
• MyVariant Identifiers: chr10:g.50669539A>G (hg19) ; chr10:g.49461493A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461493A>G , CM000672.2:g.49461493A>G	GRCh38
NC_000010.10:g.50669539A>G , CM000672.1:g.50669539A>G	GRCh37
NC_000010.9:g.50339545A>G	NCBI36
NG_009442.1:g.82609T>C , LRG_465:g.82609T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3842T>C MANE Select	ENSP00000348089.5:p.Leu1281Pro
ENST00000679552.1:n.913T>C
ENST00000679871.1:n.988T>C
ENST00000679974.1:n.891T>C
ENST00000681632.1:n.5245T>C
ENST00000681659.1:c.3683T>C	ENSP00000505631.1:p.Leu1228Pro
ENST00000355832.9:c.3842T>C	ENSP00000348089.5:p.Leu1281Pro
ENST00000465653.1:n.164T>C
ENST00000623073.3:c.*2138T>C	ENSP00000485650.1:n.*2138T>C
ENST00000623115.3:c.1952T>C	ENSP00000485321.1:p.Leu651Pro
ENST00000624341.3:c.1674T>C
NM_000124.3:c.3842T>C	NP_000115.1:p.Leu1281Pro
XR_945953.1:n.243-10072A>G
NM_001346440.1:c.3842T>C	NP_001333369.1:p.Leu1281Pro
NM_000124.4:c.3842T>C MANE Select	NP_000115.1:p.Leu1281Pro
NM_001346440.2:c.3842T>C	NP_001333369.1:p.Leu1281Pro