Canonical Allele Identifier: CA206612845
Community Standard Title: NM_000124.4(ERCC6):c.*2766T>G
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49456049A>C , CM000672.2:g.49456049A>C GRCh38
NC_000010.10:g.50664095A>C , CM000672.1:g.50664095A>C GRCh37
NC_000010.9:g.50334101A>C NCBI36
NG_009442.1:g.88053T>G , LRG_465:g.88053T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000124.4:c.*2766T>G MANE Select NP_000115.1:n.*2766T>G
ENST00000355832.10:c.*2766T>G MANE Select ENSP00000348089.5:n.*2766T>G
NM_000124.3:c.*2766T>G NP_000115.1:n.*2766T>G
NM_001346440.1:c.*2766T>G NP_001333369.1:n.*2766T>G
NM_001346440.2:c.*2766T>G NP_001333369.1:n.*2766T>G
ENST00000355832.9:c.*2766T>G ENSP00000348089.5:n.*2766T>G
ENST00000624341.3:c.5080T>G
ENST00000679871.1:n.4394T>G
ENST00000679974.1:n.4297T>G
ENST00000681632.1:n.8651T>G
ENST00000681659.1:c.*2766T>G ENSP00000505631.1:n.*2766T>G
XR_945953.1:n.243-15516A>C