Canonical Allele Identifier: CA493690095

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14041922T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948065T>C , CM000678.2:g.13948065T>C	GRCh38
NC_000016.9:g.14041922T>C , CM000678.1:g.14041922T>C	GRCh37
NC_000016.8:g.13949423T>C	NCBI36
NG_011442.1:g.32909T>C , LRG_463:g.32909T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2607T>C	ENSP00000507912.1:p.Pro869=
ENST00000683962.1:c.*2163T>C	ENSP00000506854.1:n.*2163T>C
ENST00000311895.8:c.2469T>C MANE Select	ENSP00000310520.7:p.Pro823=
ENST00000311895.7:c.2469T>C	ENSP00000310520.7:p.Pro823=
ENST00000389138.7:n.1746T>C
NM_005236.2:c.2469T>C , LRG_463t1:c.2469T>C	NP_005227.1:p.Pro823=
XM_011522424.1:c.2607T>C	XP_011520726.1:p.Pro869=
XM_011522425.1:c.1926T>C	XP_011520727.1:p.Pro642=
XM_011522426.1:c.1680T>C	XP_011520728.1:p.Pro560=
XM_011522427.1:c.1119T>C	XP_011520729.1:p.Pro373=
XR_932805.1:n.2628T>C
XM_011522424.3:c.2607T>C	XP_011520726.1:p.Pro869=
XM_017023043.2:c.1680T>C	XP_016878532.1:p.Pro560=
NM_005236.3:c.2469T>C MANE Select	NP_005227.1:p.Pro823=