Canonical Allele Identifier: CA2609141187

Gene: ERCC6

Linked Data

• gnomAD v4: 10-49528328-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49528328C>T , CM000672.2:g.49528328C>T	GRCh38
NC_000010.10:g.50736374C>T , CM000672.1:g.50736374C>T	GRCh37
NC_000010.9:g.50406380C>T	NCBI36
NG_009442.1:g.15774G>A , LRG_465:g.15774G>A
NG_033155.1:g.954G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.652+89G>A MANE Select	ENSP00000348089.5:n.652+89G>A
ENST00000447839.7:c.652+89G>A MANE Plus Clinical	ENSP00000387966.2:n.652+89G>A
ENST00000679596.1:c.*281+89G>A	ENSP00000504862.1:n.*281+89G>A
ENST00000679811.1:n.735+89G>A
ENST00000680107.1:c.652+89G>A	ENSP00000505909.1:n.652+89G>A
ENST00000680233.1:n.745+89G>A
ENST00000681632.1:n.730+89G>A
ENST00000681659.1:c.652+89G>A	ENSP00000505631.1:n.652+89G>A
ENST00000355832.9:c.652+89G>A	ENSP00000348089.5:n.652+89G>A
ENST00000447839.6:c.652+89G>A	ENSP00000387966.2:n.652+89G>A
ENST00000479652.1:n.127+89G>A
ENST00000515869.1:c.652+89G>A	ENSP00000423550.1:n.652+89G>A
NM_000124.3:c.652+89G>A	NP_000115.1:n.652+89G>A
NM_001277058.1:c.652+89G>A	NP_001263987.1:n.652+89G>A
NM_001277059.1:c.652+89G>A	NP_001263988.1:n.652+89G>A
NM_001346440.1:c.652+89G>A	NP_001333369.1:n.652+89G>A
NM_000124.4:c.652+89G>A MANE Select	NP_000115.1:n.652+89G>A
NM_001277058.2:c.652+89G>A MANE Plus Clinical	NP_001263987.1:n.652+89G>A
NM_001277059.2:c.652+89G>A	NP_001263988.1:n.652+89G>A
NM_001346440.2:c.652+89G>A	NP_001333369.1:n.652+89G>A