Canonical Allele Identifier: CA2787928462

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461571A>C , CM000672.2:g.49461571A>C	GRCh38
NC_000010.10:g.50669617A>C , CM000672.1:g.50669617A>C	GRCh37
NC_000010.9:g.50339623A>C	NCBI36
NG_009442.1:g.82531T>G , LRG_465:g.82531T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3779-15T>G MANE Select	ENSP00000348089.5:n.3779-15T>G
ENST00000679552.1:n.850-15T>G
ENST00000679871.1:n.925-15T>G
ENST00000679974.1:n.828-15T>G
ENST00000681632.1:n.5182-15T>G
ENST00000681659.1:c.3620-15T>G	ENSP00000505631.1:n.3620-15T>G
ENST00000355832.9:c.3779-15T>G	ENSP00000348089.5:n.3779-15T>G
ENST00000465653.1:n.101-15T>G
ENST00000623073.3:c.*2075-15T>G	ENSP00000485650.1:n.*2075-15T>G
ENST00000623115.3:c.1889-15T>G	ENSP00000485321.1:n.1889-15T>G
ENST00000624341.3:c.1611-15T>G
NM_000124.3:c.3779-15T>G	NP_000115.1:n.3779-15T>G
XR_945953.1:n.243-9994A>C
NM_001346440.1:c.3779-15T>G	NP_001333369.1:n.3779-15T>G
NM_000124.4:c.3779-15T>G MANE Select	NP_000115.1:n.3779-15T>G
NM_001346440.2:c.3779-15T>G	NP_001333369.1:n.3779-15T>G