Canonical Allele Identifier: CA376708676

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50669573C>T (hg19) ; chr10:g.49461527C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461527C>T , CM000672.2:g.49461527C>T	GRCh38
NC_000010.10:g.50669573C>T , CM000672.1:g.50669573C>T	GRCh37
NC_000010.9:g.50339579C>T	NCBI36
NG_009442.1:g.82575G>A , LRG_465:g.82575G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3808G>A MANE Select	ENSP00000348089.5:p.Ala1270Thr
ENST00000679552.1:n.879G>A
ENST00000679871.1:n.954G>A
ENST00000679974.1:n.857G>A
ENST00000681632.1:n.5211G>A
ENST00000681659.1:c.3649G>A	ENSP00000505631.1:p.Ala1217Thr
ENST00000355832.9:c.3808G>A	ENSP00000348089.5:p.Ala1270Thr
ENST00000465653.1:n.130G>A
ENST00000623073.3:c.*2104G>A	ENSP00000485650.1:n.*2104G>A
ENST00000623115.3:c.1918G>A	ENSP00000485321.1:p.Ala640Thr
ENST00000624341.3:c.1640G>A
NM_000124.3:c.3808G>A	NP_000115.1:p.Ala1270Thr
XR_945953.1:n.243-10038C>T
NM_001346440.1:c.3808G>A	NP_001333369.1:p.Ala1270Thr
NM_000124.4:c.3808G>A MANE Select	NP_000115.1:p.Ala1270Thr
NM_001346440.2:c.3808G>A	NP_001333369.1:p.Ala1270Thr