Canonical Allele Identifier: CA2787930322

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49493410_49493422del , CM000672.2:g.49493410_49493422del	GRCh38
NC_000010.10:g.50701456_50701468del , CM000672.1:g.50701456_50701468del	GRCh37
NC_000010.9:g.50371462_50371474del	NCBI36
NG_009442.1:g.50680_50692del , LRG_465:g.50680_50692del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.1686-170_1686-158del MANE Select	ENSP00000348089.5:n.1686-170_1686-158del
ENST00000681632.1:n.1764-170_1764-158del
ENST00000681659.1:c.1527-170_1527-158del	ENSP00000505631.1:n.1527-170_1527-158del
ENST00000355832.9:c.1686-170_1686-158del	ENSP00000348089.5:n.1686-170_1686-158del
ENST00000475116.1:n.275+7116_275+7128del
ENST00000623073.3:c.87-170_87-158del	ENSP00000485650.1:n.87-170_87-158del
ENST00000623115.3:c.-70+7116_-70+7128del	ENSP00000485321.1:n.-70+7116_-70+7128del
ENST00000623318.1:c.87-170_87-158del	ENSP00000485423.1:n.87-170_87-158del
NM_000124.3:c.1686-170_1686-158del	NP_000115.1:n.1686-170_1686-158del
NM_001346440.1:c.1686-170_1686-158del	NP_001333369.1:n.1686-170_1686-158del
NM_000124.4:c.1686-170_1686-158del MANE Select	NP_000115.1:n.1686-170_1686-158del
NM_001346440.2:c.1686-170_1686-158del	NP_001333369.1:n.1686-170_1686-158del