Canonical Allele Identifier: CA915940381
Community Standard Title: NM_000124.4(ERCC6):c.1914del (p.Tyr638Ter)
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49483424del , CM000672.2:g.49483424del GRCh38
NC_000010.10:g.50691470del , CM000672.1:g.50691470del GRCh37
NC_000010.9:g.50361476del NCBI36
NG_009442.1:g.60678del , LRG_465:g.60678del

Transcript Alleles

HGVS Amino-acid Change
NM_000124.4:c.1914del MANE Select NP_000115.1:p.Tyr638Ter
ENST00000355832.10:c.1914del MANE Select ENSP00000348089.5:p.Tyr638Ter
NM_000124.3:c.1914del NP_000115.1:p.Tyr638Ter
NM_001346440.1:c.1914del NP_001333369.1:p.Tyr638Ter
NM_001346440.2:c.1914del NP_001333369.1:p.Tyr638Ter
ENST00000355832.9:c.1914del ENSP00000348089.5:p.Tyr638Ter
ENST00000475116.1:n.368del
ENST00000623073.3:c.*306del ENSP00000485650.1:n.*306del
ENST00000623115.3:c.24del ENSP00000485321.1:p.Tyr8Ter
ENST00000623318.1:c.315del ENSP00000485423.1:p.Tyr105Ter
ENST00000681632.1:n.1992del
ENST00000681659.1:c.1755del ENSP00000505631.1:p.Tyr585Ter