Canonical Allele Identifier: CA10635841
Community Standard Title: NM_000124.4(ERCC6):c.*2155T>C
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49456660A>G , CM000672.2:g.49456660A>G GRCh38
NC_000010.10:g.50664706A>G , CM000672.1:g.50664706A>G GRCh37
NC_000010.9:g.50334712A>G NCBI36
NG_009442.1:g.87442T>C , LRG_465:g.87442T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000124.4:c.*2155T>C MANE Select NP_000115.1:n.*2155T>C
ENST00000355832.10:c.*2155T>C MANE Select ENSP00000348089.5:n.*2155T>C
NM_000124.3:c.*2155T>C NP_000115.1:n.*2155T>C
NM_001346440.1:c.*2155T>C NP_001333369.1:n.*2155T>C
NM_001346440.2:c.*2155T>C NP_001333369.1:n.*2155T>C
ENST00000355832.9:c.*2155T>C ENSP00000348089.5:n.*2155T>C
ENST00000623073.3:c.*4933T>C ENSP00000485650.1:n.*4933T>C
ENST00000624341.3:c.4469T>C
ENST00000679552.1:n.4846T>C
ENST00000679871.1:n.3783T>C
ENST00000679974.1:n.3686T>C
ENST00000681632.1:n.8040T>C
ENST00000681659.1:c.*2155T>C ENSP00000505631.1:n.*2155T>C
XR_945953.1:n.243-14905A>G