Canonical Allele Identifier: CA1908764040

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49524538C= , CM000672.2:g.49524538C=	GRCh38
NC_000010.10:g.50732584C= , CM000672.1:g.50732584C=	GRCh37
NC_000010.9:g.50402590C=	NCBI36
NG_009442.1:g.19564G= , LRG_465:g.19564G=
NG_033155.1:g.4744G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.892G= MANE Select	ENSP00000348089.5:p.Ala298=
ENST00000447839.7:c.892G= MANE Plus Clinical	ENSP00000387966.2:p.Ala298=
ENST00000679596.1:c.*521G=	ENSP00000504862.1:n.*521G=
ENST00000679811.1:n.975G=
ENST00000680107.1:c.652+3879G=	ENSP00000505909.1:n.652+3879G=
ENST00000680233.1:n.985G=
ENST00000681632.1:n.970G=
ENST00000681659.1:c.892G=	ENSP00000505631.1:p.Ala298=
ENST00000355832.9:c.892G=	ENSP00000348089.5:p.Ala298=
ENST00000447839.6:c.892G=	ENSP00000387966.2:p.Ala298=
ENST00000515869.1:c.892G=	ENSP00000423550.1:p.Ala298=
NM_000124.3:c.892G=	NP_000115.1:p.Ala298=
NM_001277058.1:c.892G=	NP_001263987.1:p.Ala298=
NM_001277059.1:c.892G=	NP_001263988.1:p.Ala298=
NM_001346440.1:c.892G=	NP_001333369.1:p.Ala298=
NM_000124.4:c.892G= MANE Select	NP_000115.1:p.Ala298=
NM_001277058.2:c.892G= MANE Plus Clinical	NP_001263987.1:p.Ala298=
NM_001277059.2:c.892G=	NP_001263988.1:p.Ala298=
NM_001346440.2:c.892G=	NP_001333369.1:p.Ala298=