Canonical Allele Identifier: CA1908750276
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49472379T= , CM000672.2:g.49472379T= GRCh38
NC_000010.10:g.50680425T= , CM000672.1:g.50680425T= GRCh37
NC_000010.9:g.50350431T= NCBI36
NG_009442.1:g.71723A= , LRG_465:g.71723A=

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.2921A= MANE Select ENSP00000348089.5:p.His974=
ENST00000681632.1:n.4324A=
ENST00000681659.1:c.2762A= ENSP00000505631.1:p.His921=
ENST00000355832.9:c.2921A= ENSP00000348089.5:p.His974=
ENST00000623073.3:c.*1217A= ENSP00000485650.1:n.*1217A=
ENST00000623115.3:c.1031A= ENSP00000485321.1:p.His344=
ENST00000624341.3:c.753A=
NM_000124.3:c.2921A= NP_000115.1:p.His974=
XR_945953.1:n.690-324T=
NM_001346440.1:c.2921A= NP_001333369.1:p.His974=
NM_000124.4:c.2921A= MANE Select NP_000115.1:p.His974=
NM_001346440.2:c.2921A= NP_001333369.1:p.His974=