Canonical Allele Identifier: CA376712404
Community Standard Title: NM_000124.4(ERCC6):c.3757G>T (p.Glu1253Ter)
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49470203C>A , CM000672.2:g.49470203C>A GRCh38
NC_000010.10:g.50678249C>A , CM000672.1:g.50678249C>A GRCh37
NC_000010.9:g.50348255C>A NCBI36
NG_009442.1:g.73899G>T , LRG_465:g.73899G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000124.4:c.3757G>T MANE Select NP_000115.1:p.Glu1253Ter
ENST00000355832.10:c.3757G>T MANE Select ENSP00000348089.5:p.Glu1253Ter
NM_000124.3:c.3757G>T NP_000115.1:p.Glu1253Ter
NM_001346440.1:c.3757G>T NP_001333369.1:p.Glu1253Ter
NM_001346440.2:c.3757G>T NP_001333369.1:p.Glu1253Ter
ENST00000355832.9:c.3757G>T ENSP00000348089.5:p.Glu1253Ter
ENST00000465653.1:n.79G>T
ENST00000623073.3:c.*2053G>T ENSP00000485650.1:n.*2053G>T
ENST00000623115.3:c.1867G>T ENSP00000485321.1:p.Glu623Ter
ENST00000624341.3:c.1589G>T
ENST00000679552.1:n.828G>T
ENST00000679871.1:n.903G>T
ENST00000679974.1:n.806G>T
ENST00000681632.1:n.5160G>T
ENST00000681659.1:c.3598G>T ENSP00000505631.1:p.Glu1200Ter
XR_945953.1:n.243-1362C>A