Canonical Allele Identifier: CA5541559

Linked Data

dbSNP Id: rs770555957

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70883914del , CM000672.2:g.70883914del GRCh38
NC_000010.10:g.72643671del , CM000672.1:g.72643671del GRCh37
NC_000010.9:g.72313677del NCBI36
NG_008646.1:g.9874del

Transcript Alleles

HGVS Amino-acid change
ENST00000697988.1:c.571-9845del (SGPL1) ENSP00000513492.1:n.571-9845del
ENST00000299299.4:c.*39del (PCBD1) MANE Select ENSP00000299299.3:n.*39del
ENST00000299299.3:c.*39del (PCBD1) ENSP00000299299.3:n.*39del
ENST00000493961.5:n.183+1241del (PCBD1)
NM_000281.3:c.*39del (PCBD1) NP_000272.1:n.*39del
NM_001289797.1:c.*39del (PCBD1) NP_001276726.1:n.*39del
XM_005269877.1:c.216+1241del (PCBD1) XP_005269934.1:n.216+1241del
NM_001323004.1:c.216+1241del (PCBD1) NP_001309933.1:n.216+1241del
NM_000281.4:c.*39del (PCBD1) MANE Select NP_000272.1:n.*39del
NM_001289797.2:c.*39del (PCBD1) NP_001276726.1:n.*39del
NM_001323004.2:c.216+1241del (PCBD1) NP_001309933.1:n.216+1241del