Canonical Allele Identifier: CA394824409

Gene: ERCC4

Linked Data

• dbSNP Id: rs2141621068
• MyVariant Identifiers: chr16:g.14041995C>G (hg19) ; chr16:g.13948138C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948138C>G , CM000678.2:g.13948138C>G	GRCh38
NC_000016.9:g.14041995C>G , CM000678.1:g.14041995C>G	GRCh37
NC_000016.8:g.13949496C>G	NCBI36
NG_011442.1:g.32982C>G , LRG_463:g.32982C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2680C>G	ENSP00000507912.1:p.Pro894Ala
ENST00000683962.1:c.*2236C>G	ENSP00000506854.1:n.*2236C>G
ENST00000311895.8:c.2542C>G MANE Select	ENSP00000310520.7:p.Pro848Ala
ENST00000311895.7:c.2542C>G	ENSP00000310520.7:p.Pro848Ala
ENST00000389138.7:n.1819C>G
NM_005236.2:c.2542C>G , LRG_463t1:c.2542C>G	NP_005227.1:p.Pro848Ala
XM_011522424.1:c.2680C>G	XP_011520726.1:p.Pro894Ala
XM_011522425.1:c.1999C>G	XP_011520727.1:p.Pro667Ala
XM_011522426.1:c.1753C>G	XP_011520728.1:p.Pro585Ala
XM_011522427.1:c.1192C>G	XP_011520729.1:p.Pro398Ala
XR_932805.1:n.2701C>G
XM_011522424.3:c.2680C>G	XP_011520726.1:p.Pro894Ala
XM_017023043.2:c.1753C>G	XP_016878532.1:p.Pro585Ala
NM_005236.3:c.2542C>G MANE Select	NP_005227.1:p.Pro848Ala