Canonical Allele Identifier: CA1908752999
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49514807_49514808delinsAT , CM000672.2:g.49514807_49514808delinsAT GRCh38
NC_000010.10:g.50722853_50722854delinsAT , CM000672.1:g.50722853_50722854delinsAT GRCh37
NC_000010.9:g.50392859_50392860delinsAT NCBI36
NG_009442.1:g.29294_29295delinsAT , LRG_465:g.29294_29295delinsAT
NG_033155.1:g.14474_14475delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.1398-8796_1398-8795delinsAT MANE Select ENSP00000348089.5:n.1398-8796_1398-8795de...
ENST00000679811.1:n.1481-8796_1481-8795delinsAT
ENST00000680107.1:c.*2291_*2292delinsAT ENSP00000505909.1:n.*2291_*2292delinsAT
ENST00000681632.1:n.1476-8796_1476-8795delinsAT
ENST00000681659.1:c.1398-8796_1398-8795delinsAT ENSP00000505631.1:n.1398-8796_1398-8795de...
ENST00000355832.9:c.1398-8796_1398-8795delinsAT ENSP00000348089.5:n.1398-8796_1398-8795de...
NM_000124.3:c.1398-8796_1398-8795delinsAT NP_000115.1:n.1398-8796_1398-8795delinsAT...
NM_001346440.1:c.1398-8796_1398-8795delinsAT NP_001333369.1:n.1398-8796_1398-8795delin...
NM_000124.4:c.1398-8796_1398-8795delinsAT MANE Select NP_000115.1:n.1398-8796_1398-8795delinsAT...
NM_001346440.2:c.1398-8796_1398-8795delinsAT NP_001333369.1:n.1398-8796_1398-8795delin...