Canonical Allele Identifier: CA469600276

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50669421A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461375A>T , CM000672.2:g.49461375A>T	GRCh38
NC_000010.10:g.50669421A>T , CM000672.1:g.50669421A>T	GRCh37
NC_000010.9:g.50339427A>T	NCBI36
NG_009442.1:g.82727T>A , LRG_465:g.82727T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.3960T>A MANE Select	ENSP00000348089.5:p.Ile1320=
ENST00000679552.1:n.1031T>A
ENST00000679871.1:n.1106T>A
ENST00000679974.1:n.1009T>A
ENST00000681632.1:n.5363T>A
ENST00000681659.1:c.3801T>A	ENSP00000505631.1:p.Ile1267=
ENST00000355832.9:c.3960T>A	ENSP00000348089.5:p.Ile1320=
ENST00000465653.1:n.282T>A
ENST00000623073.3:c.*2256T>A	ENSP00000485650.1:n.*2256T>A
ENST00000623115.3:c.2070T>A	ENSP00000485321.1:p.Ile690=
ENST00000624341.3:c.1792T>A
NM_000124.3:c.3960T>A	NP_000115.1:p.Ile1320=
XR_945953.1:n.243-10190A>T
NM_001346440.1:c.3960T>A	NP_001333369.1:p.Ile1320=
NM_000124.4:c.3960T>A MANE Select	NP_000115.1:p.Ile1320=
NM_001346440.2:c.3960T>A	NP_001333369.1:p.Ile1320=