Canonical Allele Identifier: CA469790479

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50732579T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49524533T>A , CM000672.2:g.49524533T>A	GRCh38
NC_000010.10:g.50732579T>A , CM000672.1:g.50732579T>A	GRCh37
NC_000010.9:g.50402585T>A	NCBI36
NG_009442.1:g.19569A>T , LRG_465:g.19569A>T
NG_033155.1:g.4749A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.897A>T MANE Select	ENSP00000348089.5:p.Pro299=
ENST00000447839.7:c.897A>T MANE Plus Clinical	ENSP00000387966.2:p.Pro299=
ENST00000679596.1:c.*526A>T	ENSP00000504862.1:n.*526A>T
ENST00000679811.1:n.980A>T
ENST00000680107.1:c.652+3884A>T	ENSP00000505909.1:n.652+3884A>T
ENST00000680233.1:n.990A>T
ENST00000681632.1:n.975A>T
ENST00000681659.1:c.897A>T	ENSP00000505631.1:p.Pro299=
ENST00000355832.9:c.897A>T	ENSP00000348089.5:p.Pro299=
ENST00000447839.6:c.897A>T	ENSP00000387966.2:p.Pro299=
ENST00000515869.1:c.897A>T	ENSP00000423550.1:p.Pro299=
NM_000124.3:c.897A>T	NP_000115.1:p.Pro299=
NM_001277058.1:c.897A>T	NP_001263987.1:p.Pro299=
NM_001277059.1:c.897A>T	NP_001263988.1:p.Pro299=
NM_001346440.1:c.897A>T	NP_001333369.1:p.Pro299=
NM_000124.4:c.897A>T MANE Select	NP_000115.1:p.Pro299=
NM_001277058.2:c.897A>T MANE Plus Clinical	NP_001263987.1:p.Pro299=
NM_001277059.2:c.897A>T	NP_001263988.1:p.Pro299=
NM_001346440.2:c.897A>T	NP_001333369.1:p.Pro299=