Canonical Allele Identifier: CA206612692

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49455869G>A , CM000672.2:g.49455869G>A	GRCh38
NC_000010.10:g.50663915G>A , CM000672.1:g.50663915G>A	GRCh37
NC_000010.9:g.50333921G>A	NCBI36
NG_009442.1:g.88233C>T , LRG_465:g.88233C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.*2946C>T MANE Select	ENSP00000348089.5:n.*2946C>T
ENST00000679871.1:n.4574C>T
ENST00000679974.1:n.4477C>T
ENST00000681632.1:n.8831C>T
ENST00000681659.1:c.*2946C>T	ENSP00000505631.1:n.*2946C>T
ENST00000355832.9:c.*2946C>T	ENSP00000348089.5:n.*2946C>T
ENST00000624341.3:c.5260C>T
NM_000124.3:c.*2946C>T	NP_000115.1:n.*2946C>T
XR_945953.1:n.243-15696G>A
NM_001346440.1:c.*2946C>T	NP_001333369.1:n.*2946C>T
NM_000124.4:c.*2946C>T MANE Select	NP_000115.1:n.*2946C>T
NM_001346440.2:c.*2946C>T	NP_001333369.1:n.*2946C>T