Canonical Allele Identifier: CA376713159

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470323T>A , CM000672.2:g.49470323T>A	GRCh38
NC_000010.10:g.50678369T>A , CM000672.1:g.50678369T>A	GRCh37
NC_000010.9:g.50348375T>A	NCBI36
NG_009442.1:g.73779A>T , LRG_465:g.73779A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000124.4:c.3637A>T MANE Select	NP_000115.1:p.Arg1213Ter
ENST00000355832.10:c.3637A>T MANE Select	ENSP00000348089.5:p.Arg1213Ter
NM_000124.3:c.3637A>T	NP_000115.1:p.Arg1213Ter
NM_001346440.1:c.3637A>T	NP_001333369.1:p.Arg1213Ter
NM_001346440.2:c.3637A>T	NP_001333369.1:p.Arg1213Ter
ENST00000355832.9:c.3637A>T	ENSP00000348089.5:p.Arg1213Ter
ENST00000623073.3:c.*1933A>T	ENSP00000485650.1:n.*1933A>T
ENST00000623115.3:c.1747A>T	ENSP00000485321.1:p.Arg583Ter
ENST00000624341.3:c.1469A>T
ENST00000679552.1:n.708A>T
ENST00000679871.1:n.783A>T
ENST00000679974.1:n.686A>T
ENST00000681632.1:n.5040A>T
ENST00000681659.1:c.3478A>T	ENSP00000505631.1:p.Arg1160Ter
XR_945953.1:n.243-1242T>A