Canonical Allele Identifier: CA432003268

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240456086T>A , CM000664.2:g.240456086T>A GRCh38
NC_000002.11:g.241395503T>A , CM000664.1:g.241395503T>A GRCh37
NC_000002.10:g.241044176T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264039.7:c.167-2944T>A (GPC1) MANE Select ENSP00000264039.2:n.167-2944T>A
ENST00000264039.6:c.167-2944T>A (GPC1) ENSP00000264039.2:n.167-2944T>A
ENST00000420138.5:c.-50-2944T>A (GPC1) ENSP00000415077.2:n.-50-2944T>A
ENST00000426280.3:c.16+1066T>A (GPC1) ENSP00000410251.1:n.16+1066T>A
ENST00000469694.5:n.181-2944T>A (GPC1)
NM_002081.2:c.167-2944T>A (GPC1) NP_002072.2:n.167-2944T>A
NR_024014.1:n.104+511A>T (GPC1-AS1)
NR_029702.1:n.86T>A (MIR149)
NM_001359125.1:c.67+511A>T (GPC1-AS1) NP_001346054.1:n.67+511A>T
NM_002081.3:c.167-2944T>A (GPC1) MANE Select NP_002072.2:n.167-2944T>A
NR_161169.1:n.104+511A>T (GPC1-AS1)