Canonical Allele Identifier: CA287477067

Gene: SENP3 SENP3-EIF4A1

Linked Data

• dbSNP Id: rs11078697
• gnomAD v3: 17-7565912-C-G
• gnomAD v4: 17-7565912-C-G
• MyVariant Identifiers: chr17:g.7469229C>G (hg19) ; chr17:g.7565912C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7565912C>G , CM000679.2:g.7565912C>G	GRCh38
NC_000017.10:g.7469229C>G , CM000679.1:g.7469229C>G	GRCh37
NC_000017.9:g.7409953C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000321337.12:c.1263+148C>G (SENP3) MANE Select	ENSP00000314029.8:n.1263+148C>G
ENST00000321337.11:c.1263+148C>G (SENP3)	ENSP00000314029.8:n.1263+148C>G
ENST00000429205.6:c.1263+148C>G (SENP3)	ENSP00000403712.2:n.1263+148C>G
ENST00000580231.5:c.330+148C>G (SENP3)	ENSP00000463358.1:n.330+148C>G
ENST00000580997.1:n.540C>G (SENP3)
ENST00000583277.1:n.1457C>G (SENP3)
ENST00000614237.1:c.1053+148C>G (SENP3-EIF4A1)	ENSP00000483614.1:n.1053+148C>G
ENST00000619785.1:c.194+148C>G (SENP3)
NM_015670.5:c.1263+148C>G (SENP3)	NP_056485.2:n.1263+148C>G
NR_037926.1:n.1546+148C>G (SENP3-EIF4A1)
NM_015670.6:c.1263+148C>G (SENP3) MANE Select	NP_056485.2:n.1263+148C>G