Canonical Allele Identifier: CA493689520

Gene: ERCC4

Linked Data

• gnomAD v4: 16-13935627-T-C
• MyVariant Identifiers: chr16:g.14029484T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935627T>C , CM000678.2:g.13935627T>C	GRCh38
NC_000016.9:g.14029484T>C , CM000678.1:g.14029484T>C	GRCh37
NC_000016.8:g.13936985T>C	NCBI36
NG_011442.1:g.20471T>C , LRG_463:g.20471T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1773T>C
ENST00000682617.1:c.1833T>C	ENSP00000507912.1:p.Ala611=
ENST00000682826.1:c.*1009T>C	ENSP00000507274.1:n.*1009T>C
ENST00000682909.1:n.3735T>C
ENST00000683277.1:n.3340T>C
ENST00000683407.1:n.1703T>C
ENST00000683962.1:c.*1389T>C	ENSP00000506854.1:n.*1389T>C
ENST00000311895.8:c.1695T>C MANE Select	ENSP00000310520.7:p.Ala565=
ENST00000311895.7:c.1695T>C	ENSP00000310520.7:p.Ala565=
ENST00000389138.7:n.972T>C
NM_005236.2:c.1695T>C , LRG_463t1:c.1695T>C	NP_005227.1:p.Ala565=
XM_011522424.1:c.1833T>C	XP_011520726.1:p.Ala611=
XM_011522425.1:c.1152T>C	XP_011520727.1:p.Ala384=
XM_011522426.1:c.906T>C	XP_011520728.1:p.Ala302=
XM_011522427.1:c.345T>C	XP_011520729.1:p.Ala115=
XR_932805.1:n.1854T>C
XM_011522424.3:c.1833T>C	XP_011520726.1:p.Ala611=
XM_017023043.2:c.906T>C	XP_016878532.1:p.Ala302=
NM_005236.3:c.1695T>C MANE Select	NP_005227.1:p.Ala565=