Canonical Allele Identifier: CA349324784

Gene: SP3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173955601T>C , CM000664.2:g.173955601T>C	GRCh38
NC_000002.11:g.174820329T>C , CM000664.1:g.174820329T>C	GRCh37
NC_000002.10:g.174528575T>C	NCBI36
NG_029153.1:g.15102A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310015.12:c.911A>G MANE Select	ENSP00000310301.6:p.Asp304Gly
ENST00000310015.11:c.911A>G	ENSP00000310301.6:p.Asp304Gly
ENST00000418194.7:c.707A>G	ENSP00000406140.3:p.Asp236Gly
ENST00000650743.1:c.632A>G	ENSP00000498794.1:p.Asp211Gly
ENST00000652005.2:c.707A>G	ENSP00000498392.2:p.Asp236Gly
ENST00000310015.10:c.911A>G	ENSP00000310301.6:p.Asp304Gly
ENST00000416195.1:c.781A>G
ENST00000418194.6:c.707A>G	ENSP00000406140.2:p.Asp236Gly
NM_001017371.4:c.707A>G	NP_001017371.3:p.Asp236Gly
NM_001172712.1:c.902A>G	NP_001166183.1:p.Asp301Gly
NM_003111.4:c.911A>G	NP_003102.1:p.Asp304Gly
NM_001017371.5:c.707A>G	NP_001017371.3:p.Asp236Gly
NM_003111.5:c.911A>G MANE Select	NP_003102.1:p.Asp304Gly