Canonical Allele Identifier: CA1908745498

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461449C= , CM000672.2:g.49461449C=	GRCh38
NC_000010.10:g.50669495C= , CM000672.1:g.50669495C=	GRCh37
NC_000010.9:g.50339501C=	NCBI36
NG_009442.1:g.82653G= , LRG_465:g.82653G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3886G= MANE Select	ENSP00000348089.5:p.Ala1296=
ENST00000679552.1:n.957G=
ENST00000679871.1:n.1032G=
ENST00000679974.1:n.935G=
ENST00000681632.1:n.5289G=
ENST00000681659.1:c.3727G=	ENSP00000505631.1:p.Ala1243=
ENST00000355832.9:c.3886G=	ENSP00000348089.5:p.Ala1296=
ENST00000465653.1:n.208G=
ENST00000623073.3:c.*2182G=	ENSP00000485650.1:n.*2182G=
ENST00000623115.3:c.1996G=	ENSP00000485321.1:p.Ala666=
ENST00000624341.3:c.1718G=
NM_000124.3:c.3886G=	NP_000115.1:p.Ala1296=
XR_945953.1:n.243-10116C=
NM_001346440.1:c.3886G=	NP_001333369.1:p.Ala1296=
NM_000124.4:c.3886G= MANE Select	NP_000115.1:p.Ala1296=
NM_001346440.2:c.3886G=	NP_001333369.1:p.Ala1296=