Canonical Allele Identifier: CA1908749355
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49470341T= , CM000672.2:g.49470341T= GRCh38
NC_000010.10:g.50678387T= , CM000672.1:g.50678387T= GRCh37
NC_000010.9:g.50348393T= NCBI36
NG_009442.1:g.73761A= , LRG_465:g.73761A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355832.10:c.3619A= MANE Select ENSP00000348089.5:p.Lys1207=
ENST00000679552.1:n.690A=
ENST00000679871.1:n.765A=
ENST00000679974.1:n.668A=
ENST00000681632.1:n.5022A=
ENST00000681659.1:c.3460A= ENSP00000505631.1:p.Lys1154=
ENST00000355832.9:c.3619A= ENSP00000348089.5:p.Lys1207=
ENST00000623073.3:c.*1915A= ENSP00000485650.1:n.*1915A=
ENST00000623115.3:c.1729A= ENSP00000485321.1:p.Lys577=
ENST00000624341.3:c.1451A=
NM_000124.3:c.3619A= NP_000115.1:p.Lys1207=
XR_945953.1:n.243-1224T=
NM_001346440.1:c.3619A= NP_001333369.1:p.Lys1207=
NM_000124.4:c.3619A= MANE Select NP_000115.1:p.Lys1207=
NM_001346440.2:c.3619A= NP_001333369.1:p.Lys1207=