Canonical Allele Identifier: CA1908752983
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49514768T= , CM000672.2:g.49514768T= GRCh38
NC_000010.10:g.50722814T= , CM000672.1:g.50722814T= GRCh37
NC_000010.9:g.50392820T= NCBI36
NG_009442.1:g.29334A= , LRG_465:g.29334A=
NG_033155.1:g.14514A=

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.1398-8756A= MANE Select ENSP00000348089.5:n.1398-8756A=
ENST00000679811.1:n.1481-8756A=
ENST00000680107.1:c.*2331A= ENSP00000505909.1:n.*2331A=
ENST00000681632.1:n.1476-8756A=
ENST00000681659.1:c.1398-8756A= ENSP00000505631.1:n.1398-8756A=
ENST00000355832.9:c.1398-8756A= ENSP00000348089.5:n.1398-8756A=
NM_000124.3:c.1398-8756A= NP_000115.1:n.1398-8756A=
NM_001346440.1:c.1398-8756A= NP_001333369.1:n.1398-8756A=
NM_000124.4:c.1398-8756A= MANE Select NP_000115.1:n.1398-8756A=
NM_001346440.2:c.1398-8756A= NP_001333369.1:n.1398-8756A=