Canonical Allele Identifier: CA1908752994
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49514794_49514795delinsTG , CM000672.2:g.49514794_49514795delinsTG GRCh38
NC_000010.10:g.50722840_50722841delinsTG , CM000672.1:g.50722840_50722841delinsTG GRCh37
NC_000010.9:g.50392846_50392847delinsTG NCBI36
NG_009442.1:g.29307_29308delinsCA , LRG_465:g.29307_29308delinsCA
NG_033155.1:g.14487_14488delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.1398-8783_1398-8782delinsCA MANE Select ENSP00000348089.5:n.1398-8783_1398-8782de...
ENST00000679811.1:n.1481-8783_1481-8782delinsCA
ENST00000680107.1:c.*2304_*2305delinsCA ENSP00000505909.1:n.*2304_*2305delinsCA
ENST00000681632.1:n.1476-8783_1476-8782delinsCA
ENST00000681659.1:c.1398-8783_1398-8782delinsCA ENSP00000505631.1:n.1398-8783_1398-8782de...
ENST00000355832.9:c.1398-8783_1398-8782delinsCA ENSP00000348089.5:n.1398-8783_1398-8782de...
NM_000124.3:c.1398-8783_1398-8782delinsCA NP_000115.1:n.1398-8783_1398-8782delinsCA...
NM_001346440.1:c.1398-8783_1398-8782delinsCA NP_001333369.1:n.1398-8783_1398-8782delin...
NM_000124.4:c.1398-8783_1398-8782delinsCA MANE Select NP_000115.1:n.1398-8783_1398-8782delinsCA...
NM_001346440.2:c.1398-8783_1398-8782delinsCA NP_001333369.1:n.1398-8783_1398-8782delin...