Canonical Allele Identifier: CA2787930240
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49493287A>C , CM000672.2:g.49493287A>C GRCh38
NC_000010.10:g.50701333A>C , CM000672.1:g.50701333A>C GRCh37
NC_000010.9:g.50371339A>C NCBI36
NG_009442.1:g.50815T>G , LRG_465:g.50815T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355832.10:c.1686-35T>G MANE Select ENSP00000348089.5:n.1686-35T>G
ENST00000681632.1:n.1764-35T>G
ENST00000681659.1:c.1527-35T>G ENSP00000505631.1:n.1527-35T>G
ENST00000355832.9:c.1686-35T>G ENSP00000348089.5:n.1686-35T>G
ENST00000475116.1:n.275+7251T>G
ENST00000623073.3:c.87-35T>G ENSP00000485650.1:n.87-35T>G
ENST00000623115.3:c.-70+7251T>G ENSP00000485321.1:n.-70+7251T>G
ENST00000623318.1:c.87-35T>G ENSP00000485423.1:n.87-35T>G
NM_000124.3:c.1686-35T>G NP_000115.1:n.1686-35T>G
NM_001346440.1:c.1686-35T>G NP_001333369.1:n.1686-35T>G
NM_000124.4:c.1686-35T>G MANE Select NP_000115.1:n.1686-35T>G
NM_001346440.2:c.1686-35T>G NP_001333369.1:n.1686-35T>G