Canonical Allele Identifier: CA1908750328
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49472498A= , CM000672.2:g.49472498A= GRCh38
NC_000010.10:g.50680544A= , CM000672.1:g.50680544A= GRCh37
NC_000010.9:g.50350550A= NCBI36
NG_009442.1:g.71604T= , LRG_465:g.71604T=

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.2830-28T= MANE Select ENSP00000348089.5:n.2830-28T=
ENST00000681632.1:n.4205T=
ENST00000681659.1:c.2671-28T= ENSP00000505631.1:n.2671-28T=
ENST00000355832.9:c.2830-28T= ENSP00000348089.5:n.2830-28T=
ENST00000623073.3:c.*1126-28T= ENSP00000485650.1:n.*1126-28T=
ENST00000623115.3:c.940-28T= ENSP00000485321.1:n.940-28T=
ENST00000624341.3:c.662-28T=
NM_000124.3:c.2830-28T= NP_000115.1:n.2830-28T=
XR_945953.1:n.690-205A=
NM_001346440.1:c.2830-28T= NP_001333369.1:n.2830-28T=
NM_000124.4:c.2830-28T= MANE Select NP_000115.1:n.2830-28T=
NM_001346440.2:c.2830-28T= NP_001333369.1:n.2830-28T=