Canonical Allele Identifier: CA2787928502

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461646_49461647insGAT , CM000672.2:g.49461646_49461647insGAT	GRCh38
NC_000010.10:g.50669692_50669693insGAT , CM000672.1:g.50669692_50669693insGAT	GRCh37
NC_000010.9:g.50339698_50339699insGAT	NCBI36
NG_009442.1:g.82455_82456insATC , LRG_465:g.82455_82456insATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3779-91_3779-90insATC MANE Select	ENSP00000348089.5:n.3779-91_3779-90insATC
ENST00000679552.1:n.850-91_850-90insATC
ENST00000679871.1:n.925-91_925-90insATC
ENST00000679974.1:n.828-91_828-90insATC
ENST00000681632.1:n.5182-91_5182-90insATC
ENST00000681659.1:c.3620-91_3620-90insATC	ENSP00000505631.1:n.3620-91_3620-90insATC
ENST00000355832.9:c.3779-91_3779-90insATC	ENSP00000348089.5:n.3779-91_3779-90insATC
ENST00000465653.1:n.101-91_101-90insATC
ENST00000623073.3:c.*2075-91_*2075-90insATC	ENSP00000485650.1:n.*2075-91_*2075-90insATC
ENST00000623115.3:c.1889-91_1889-90insATC	ENSP00000485321.1:n.1889-91_1889-90insATC
ENST00000624341.3:c.1611-91_1611-90insATC
NM_000124.3:c.3779-91_3779-90insATC	NP_000115.1:n.3779-91_3779-90insATC
XR_945953.1:n.243-9919_243-9918insGAT
NM_001346440.1:c.3779-91_3779-90insATC	NP_001333369.1:n.3779-91_3779-90insATC
NM_000124.4:c.3779-91_3779-90insATC MANE Select	NP_000115.1:n.3779-91_3779-90insATC
NM_001346440.2:c.3779-91_3779-90insATC	NP_001333369.1:n.3779-91_3779-90insATC