Canonical Allele Identifier: CA377127251

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70884004T>G , CM000672.2:g.70884004T>G GRCh38
NC_000010.10:g.72643761T>G , CM000672.1:g.72643761T>G GRCh37
NC_000010.9:g.72313767T>G NCBI36
NG_008646.1:g.9781A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000697988.1:c.571-9755T>G (SGPL1) ENSP00000513492.1:n.571-9755T>G
ENST00000299299.4:c.261A>C (PCBD1) MANE Select ENSP00000299299.3:p.Glu87Asp
ENST00000299299.3:c.261A>C (PCBD1) ENSP00000299299.3:p.Glu87Asp
ENST00000493228.1:n.660A>C (PCBD1)
ENST00000493961.5:n.183+1148A>C (PCBD1)
NM_000281.3:c.261A>C (PCBD1) NP_000272.1:p.Glu87Asp
NM_001289797.1:c.114A>C (PCBD1) NP_001276726.1:p.Glu38Asp
XM_005269877.1:c.216+1148A>C (PCBD1) XP_005269934.1:n.216+1148A>C
NM_001323004.1:c.216+1148A>C (PCBD1) NP_001309933.1:n.216+1148A>C
NM_000281.4:c.261A>C (PCBD1) MANE Select NP_000272.1:p.Glu87Asp
NM_001289797.2:c.114A>C (PCBD1) NP_001276726.1:p.Glu38Asp
NM_001323004.2:c.216+1148A>C (PCBD1) NP_001309933.1:n.216+1148A>C