Canonical Allele Identifier: CA287477068

Gene: SENP3 SENP3-EIF4A1

Linked Data

• dbSNP Id: rs933227688
• gnomAD v2: 17-7469230-G-A
• gnomAD v3: 17-7565913-G-A
• gnomAD v4: 17-7565913-G-A
• MyVariant Identifiers: chr17:g.7469230G>A (hg19) ; chr17:g.7565913G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7565913G>A , CM000679.2:g.7565913G>A	GRCh38
NC_000017.10:g.7469230G>A , CM000679.1:g.7469230G>A	GRCh37
NC_000017.9:g.7409954G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000321337.12:c.1263+149G>A (SENP3) MANE Select	ENSP00000314029.8:n.1263+149G>A
ENST00000321337.11:c.1263+149G>A (SENP3)	ENSP00000314029.8:n.1263+149G>A
ENST00000429205.6:c.1263+149G>A (SENP3)	ENSP00000403712.2:n.1263+149G>A
ENST00000580231.5:c.330+149G>A (SENP3)	ENSP00000463358.1:n.330+149G>A
ENST00000580997.1:n.541G>A (SENP3)
ENST00000583277.1:n.1458G>A (SENP3)
ENST00000614237.1:c.1053+149G>A (SENP3-EIF4A1)	ENSP00000483614.1:n.1053+149G>A
ENST00000619785.1:c.194+149G>A (SENP3)
NM_015670.5:c.1263+149G>A (SENP3)	NP_056485.2:n.1263+149G>A
NR_037926.1:n.1546+149G>A (SENP3-EIF4A1)
NM_015670.6:c.1263+149G>A (SENP3) MANE Select	NP_056485.2:n.1263+149G>A