Canonical Allele Identifier: CA1908744539
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49459242A= , CM000672.2:g.49459242A= GRCh38
NC_000010.10:g.50667288A= , CM000672.1:g.50667288A= GRCh37
NC_000010.9:g.50337294A= NCBI36
NG_009442.1:g.84860T= , LRG_465:g.84860T=

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.4063-8T= MANE Select ENSP00000348089.5:n.4063-8T=
ENST00000679552.1:n.2264T=
ENST00000679871.1:n.1209-8T=
ENST00000679974.1:n.1112-8T=
ENST00000681632.1:n.5466-8T=
ENST00000681659.1:c.3904-8T= ENSP00000505631.1:n.3904-8T=
ENST00000355832.9:c.4063-8T= ENSP00000348089.5:n.4063-8T=
ENST00000623073.3:c.*2359-8T= ENSP00000485650.1:n.*2359-8T=
ENST00000623115.3:c.2173-8T= ENSP00000485321.1:n.2173-8T=
ENST00000624341.3:c.1895-8T=
NM_000124.3:c.4063-8T= NP_000115.1:n.4063-8T=
XR_945953.1:n.243-12323A=
NM_001346440.1:c.4063-8T= NP_001333369.1:n.4063-8T=
NM_000124.4:c.4063-8T= MANE Select NP_000115.1:n.4063-8T=
NM_001346440.2:c.4063-8T= NP_001333369.1:n.4063-8T=