Canonical Allele Identifier: CA7910784
Gene: ERCC4 HGNC NCBI

Linked Data

dbSNP Id: rs778153718

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948228G>T , CM000678.2:g.13948228G>T GRCh38
NC_000016.9:g.14042085G>T , CM000678.1:g.14042085G>T GRCh37
NC_000016.8:g.13949586G>T NCBI36
NG_011442.1:g.33072G>T , LRG_463:g.33072G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2770G>T ENSP00000507912.1:p.Ala924Ser
ENST00000683962.1:c.*2326G>T ENSP00000506854.1:n.*2326G>T
ENST00000311895.8:c.2632G>T MANE Select ENSP00000310520.7:p.Ala878Ser
ENST00000311895.7:c.2632G>T ENSP00000310520.7:p.Ala878Ser
ENST00000389138.7:n.1909G>T
NM_005236.2:c.2632G>T , LRG_463t1:c.2632G>T NP_005227.1:p.Ala878Ser
XM_011522424.1:c.2770G>T XP_011520726.1:p.Ala924Ser
XM_011522425.1:c.2089G>T XP_011520727.1:p.Ala697Ser
XM_011522426.1:c.1843G>T XP_011520728.1:p.Ala615Ser
XM_011522427.1:c.1282G>T XP_011520729.1:p.Ala428Ser
XR_932805.1:n.2791G>T
XM_011522424.3:c.2770G>T XP_011520726.1:p.Ala924Ser
XM_017023043.2:c.1843G>T XP_016878532.1:p.Ala615Ser
NM_005236.3:c.2632G>T MANE Select NP_005227.1:p.Ala878Ser