Canonical Allele Identifier: CA1908753003
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49514813G= , CM000672.2:g.49514813G= GRCh38
NC_000010.10:g.50722859G= , CM000672.1:g.50722859G= GRCh37
NC_000010.9:g.50392865G= NCBI36
NG_009442.1:g.29289C= , LRG_465:g.29289C=
NG_033155.1:g.14469C=

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.1398-8801C= MANE Select ENSP00000348089.5:n.1398-8801C=
ENST00000679811.1:n.1481-8801C=
ENST00000680107.1:c.*2286C= ENSP00000505909.1:n.*2286C=
ENST00000681632.1:n.1476-8801C=
ENST00000681659.1:c.1398-8801C= ENSP00000505631.1:n.1398-8801C=
ENST00000355832.9:c.1398-8801C= ENSP00000348089.5:n.1398-8801C=
NM_000124.3:c.1398-8801C= NP_000115.1:n.1398-8801C=
NM_001346440.1:c.1398-8801C= NP_001333369.1:n.1398-8801C=
NM_000124.4:c.1398-8801C= MANE Select NP_000115.1:n.1398-8801C=
NM_001346440.2:c.1398-8801C= NP_001333369.1:n.1398-8801C=