Canonical Allele Identifier: CA1908749408
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49470430T= , CM000672.2:g.49470430T= GRCh38
NC_000010.10:g.50678476T= , CM000672.1:g.50678476T= GRCh37
NC_000010.9:g.50348482T= NCBI36
NG_009442.1:g.73672A= , LRG_465:g.73672A=

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.3530A= MANE Select ENSP00000348089.5:p.Asn1177=
ENST00000679552.1:n.601A=
ENST00000679871.1:n.676A=
ENST00000679974.1:n.579A=
ENST00000681632.1:n.4933A=
ENST00000681659.1:c.3371A= ENSP00000505631.1:p.Asn1124=
ENST00000355832.9:c.3530A= ENSP00000348089.5:p.Asn1177=
ENST00000623073.3:c.*1826A= ENSP00000485650.1:n.*1826A=
ENST00000623115.3:c.1640A= ENSP00000485321.1:p.Asn547=
ENST00000624341.3:c.1362A=
NM_000124.3:c.3530A= NP_000115.1:p.Asn1177=
XR_945953.1:n.243-1135T=
NM_001346440.1:c.3530A= NP_001333369.1:p.Asn1177=
NM_000124.4:c.3530A= MANE Select NP_000115.1:p.Asn1177=
NM_001346440.2:c.3530A= NP_001333369.1:p.Asn1177=