Canonical Allele Identifier: CA377127141

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70883952A>T , CM000672.2:g.70883952A>T GRCh38
NC_000010.10:g.72643709A>T , CM000672.1:g.72643709A>T GRCh37
NC_000010.9:g.72313715A>T NCBI36
NG_008646.1:g.9833T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000697988.1:c.571-9807A>T (SGPL1) ENSP00000513492.1:n.571-9807A>T
ENST00000299299.4:c.313T>A (PCBD1) MANE Select ENSP00000299299.3:p.Ter105Lys
ENST00000299299.3:c.313T>A (PCBD1) ENSP00000299299.3:p.Ter105Lys
ENST00000493228.1:n.712T>A (PCBD1)
ENST00000493961.5:n.183+1200T>A (PCBD1)
NM_000281.3:c.313T>A (PCBD1) NP_000272.1:p.Ter105Lys
NM_001289797.1:c.166T>A (PCBD1) NP_001276726.1:p.Ter56Lys
XM_005269877.1:c.216+1200T>A (PCBD1) XP_005269934.1:n.216+1200T>A
NM_001323004.1:c.216+1200T>A (PCBD1) NP_001309933.1:n.216+1200T>A
NM_000281.4:c.313T>A (PCBD1) MANE Select NP_000272.1:p.Ter105Lys
NM_001289797.2:c.166T>A (PCBD1) NP_001276726.1:p.Ter56Lys
NM_001323004.2:c.216+1200T>A (PCBD1) NP_001309933.1:n.216+1200T>A