Canonical Allele Identifier: CA1908744542
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49459252C= , CM000672.2:g.49459252C= GRCh38
NC_000010.10:g.50667298C= , CM000672.1:g.50667298C= GRCh37
NC_000010.9:g.50337304C= NCBI36
NG_009442.1:g.84850G= , LRG_465:g.84850G=

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.4063-18G= MANE Select ENSP00000348089.5:n.4063-18G=
ENST00000679552.1:n.2254G=
ENST00000679871.1:n.1209-18G=
ENST00000679974.1:n.1112-18G=
ENST00000681632.1:n.5466-18G=
ENST00000681659.1:c.3904-18G= ENSP00000505631.1:n.3904-18G=
ENST00000355832.9:c.4063-18G= ENSP00000348089.5:n.4063-18G=
ENST00000623073.3:c.*2359-18G= ENSP00000485650.1:n.*2359-18G=
ENST00000623115.3:c.2173-18G= ENSP00000485321.1:n.2173-18G=
ENST00000624341.3:c.1895-18G=
NM_000124.3:c.4063-18G= NP_000115.1:n.4063-18G=
XR_945953.1:n.243-12313C=
NM_001346440.1:c.4063-18G= NP_001333369.1:n.4063-18G=
NM_000124.4:c.4063-18G= MANE Select NP_000115.1:n.4063-18G=
NM_001346440.2:c.4063-18G= NP_001333369.1:n.4063-18G=