Canonical Allele Identifier: CA915945907

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49538959C>A , CM000672.2:g.49538959C>A	GRCh38
NC_000010.10:g.50747005C>A , CM000672.1:g.50747005C>A	GRCh37
NC_000010.9:g.50417011C>A	NCBI36
NG_009442.1:g.5143G>T , LRG_465:g.5143G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000124.4:c.-15+3G>T MANE Select	NP_000115.1:n.-15+3G>T
ENST00000355832.10:c.-15+3G>T MANE Select	ENSP00000348089.5:n.-15+3G>T
NM_001277058.2:c.-15+3G>T MANE Plus Clinical	NP_001263987.1:n.-15+3G>T
ENST00000447839.7:c.-15+3G>T MANE Plus Clinical	ENSP00000387966.2:n.-15+3G>T
NM_000124.3:c.-15+3G>T	NP_000115.1:n.-15+3G>T
NM_001277058.1:c.-15+3G>T	NP_001263987.1:n.-15+3G>T
NM_001277059.1:c.-15+473G>T	NP_001263988.1:n.-15+473G>T
NM_001277059.2:c.-15+473G>T	NP_001263988.1:n.-15+473G>T
NM_001346440.1:c.-11+3G>T	NP_001333369.1:n.-11+3G>T
NM_001346440.2:c.-11+3G>T	NP_001333369.1:n.-11+3G>T
ENST00000355832.9:c.-15+3G>T	ENSP00000348089.5:n.-15+3G>T
ENST00000447839.6:c.-15+3G>T	ENSP00000387966.2:n.-15+3G>T
ENST00000462247.1:c.-15+473G>T	ENSP00000422827.1:n.-15+473G>T
ENST00000515869.1:c.-15+473G>T	ENSP00000423550.1:n.-15+473G>T
ENST00000679596.1:c.-22+3G>T	ENSP00000504862.1:n.-22+3G>T
ENST00000679811.1:n.69+3G>T
ENST00000680107.1:c.-15+3G>T	ENSP00000505909.1:n.-15+3G>T
ENST00000680233.1:n.79+3G>T
ENST00000681632.1:n.64+3G>T
ENST00000681659.1:c.-11+3G>T	ENSP00000505631.1:n.-11+3G>T