Canonical Allele Identifier: CA376712892
Community Standard Title: NM_000124.4(ERCC6):c.3682A>T (p.Lys1228Ter)
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49470278T>A , CM000672.2:g.49470278T>A GRCh38
NC_000010.10:g.50678324T>A , CM000672.1:g.50678324T>A GRCh37
NC_000010.9:g.50348330T>A NCBI36
NG_009442.1:g.73824A>T , LRG_465:g.73824A>T

Transcript Alleles

HGVS Amino-acid Change
NM_000124.4:c.3682A>T MANE Select NP_000115.1:p.Lys1228Ter
ENST00000355832.10:c.3682A>T MANE Select ENSP00000348089.5:p.Lys1228Ter
NM_000124.3:c.3682A>T NP_000115.1:p.Lys1228Ter
NM_001346440.1:c.3682A>T NP_001333369.1:p.Lys1228Ter
NM_001346440.2:c.3682A>T NP_001333369.1:p.Lys1228Ter
ENST00000355832.9:c.3682A>T ENSP00000348089.5:p.Lys1228Ter
ENST00000465653.1:n.4A>T
ENST00000623073.3:c.*1978A>T ENSP00000485650.1:n.*1978A>T
ENST00000623115.3:c.1792A>T ENSP00000485321.1:p.Lys598Ter
ENST00000624341.3:c.1514A>T
ENST00000679552.1:n.753A>T
ENST00000679871.1:n.828A>T
ENST00000679974.1:n.731A>T
ENST00000681632.1:n.5085A>T
ENST00000681659.1:c.3523A>T ENSP00000505631.1:p.Lys1175Ter
XR_945953.1:n.243-1287T>A