Canonical Allele Identifier: CA1908772402
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49493111T= , CM000672.2:g.49493111T= GRCh38
NC_000010.10:g.50701157T= , CM000672.1:g.50701157T= GRCh37
NC_000010.9:g.50371163T= NCBI36
NG_009442.1:g.50991A= , LRG_465:g.50991A=

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.1821+6A= MANE Select ENSP00000348089.5:n.1821+6A=
ENST00000681632.1:n.1899+6A=
ENST00000681659.1:c.1662+6A= ENSP00000505631.1:n.1662+6A=
ENST00000355832.9:c.1821+6A= ENSP00000348089.5:n.1821+6A=
ENST00000475116.1:n.275+7427A=
ENST00000623073.3:c.222+6A= ENSP00000485650.1:n.222+6A=
ENST00000623115.3:c.-70+7427A= ENSP00000485321.1:n.-70+7427A=
ENST00000623318.1:c.222+6A= ENSP00000485423.1:n.222+6A=
NM_000124.3:c.1821+6A= NP_000115.1:n.1821+6A=
NM_001346440.1:c.1821+6A= NP_001333369.1:n.1821+6A=
NM_000124.4:c.1821+6A= MANE Select NP_000115.1:n.1821+6A=
NM_001346440.2:c.1821+6A= NP_001333369.1:n.1821+6A=