Canonical Allele Identifier: CA1908763308

Gene: ERCC6 PGBD3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49524188C= , CM000672.2:g.49524188C=	GRCh38
NC_000010.10:g.50732234C= , CM000672.1:g.50732234C=	GRCh37
NC_000010.9:g.50402240C=	NCBI36
NG_009442.1:g.19914G= , LRG_465:g.19914G=
NG_033155.1:g.5094G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.1242G= (ERCC6) MANE Select	ENSP00000348089.5:p.Gln414=
ENST00000447839.7:c.1242G= (ERCC6) MANE Plus Clinical	ENSP00000387966.2:p.Gln414=
ENST00000679596.1:c.*871G= (ERCC6)	ENSP00000504862.1:n.*871G=
ENST00000679811.1:n.1325G= (ERCC6)
ENST00000680107.1:c.652+4229G= (ERCC6)	ENSP00000505909.1:n.652+4229G=
ENST00000680233.1:n.1335G= (ERCC6)
ENST00000681632.1:n.1320G= (ERCC6)
ENST00000681659.1:c.1242G= (ERCC6)	ENSP00000505631.1:p.Gln414=
ENST00000355832.9:c.1242G= (ERCC6)	ENSP00000348089.5:p.Gln414=
ENST00000374127.3:c.-163G=	ENSP00000363242.3:n.-163G=
ENST00000447839.6:c.1242G=	ENSP00000387966.2:p.Gln414=
ENST00000515869.1:c.1242G=	ENSP00000423550.1:p.Gln414=
NM_000124.3:c.1242G= (ERCC6)	NP_000115.1:p.Gln414=
NM_001277058.1:c.1242G=	NP_001263987.1:p.Gln414=
NM_001277059.1:c.1242G=	NP_001263988.1:p.Gln414=
NM_170753.3:c.-163G= (PGBD3)	NP_736609.2:n.-163G=
NM_001346440.1:c.1242G= (ERCC6)	NP_001333369.1:p.Gln414=
NM_000124.4:c.1242G= (ERCC6) MANE Select	NP_000115.1:p.Gln414=
NM_001277058.2:c.1242G= (ERCC6) MANE Plus Clinical	NP_001263987.1:p.Gln414=
NM_001277059.2:c.1242G= (ERCC6)	NP_001263988.1:p.Gln414=
NM_001346440.2:c.1242G= (ERCC6)	NP_001333369.1:p.Gln414=