Canonical Allele Identifier: CA1908752998
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49514798A= , CM000672.2:g.49514798A= GRCh38
NC_000010.10:g.50722844A= , CM000672.1:g.50722844A= GRCh37
NC_000010.9:g.50392850A= NCBI36
NG_009442.1:g.29304T= , LRG_465:g.29304T=
NG_033155.1:g.14484T=

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.1398-8786T= MANE Select ENSP00000348089.5:n.1398-8786T=
ENST00000679811.1:n.1481-8786T=
ENST00000680107.1:c.*2301T= ENSP00000505909.1:n.*2301T=
ENST00000681632.1:n.1476-8786T=
ENST00000681659.1:c.1398-8786T= ENSP00000505631.1:n.1398-8786T=
ENST00000355832.9:c.1398-8786T= ENSP00000348089.5:n.1398-8786T=
NM_000124.3:c.1398-8786T= NP_000115.1:n.1398-8786T=
NM_001346440.1:c.1398-8786T= NP_001333369.1:n.1398-8786T=
NM_000124.4:c.1398-8786T= MANE Select NP_000115.1:n.1398-8786T=
NM_001346440.2:c.1398-8786T= NP_001333369.1:n.1398-8786T=