Canonical Allele Identifier: CA278138

Linked Data

ClinVar Variation Id: 16797
ClinVar RCV Id: RCV000018288
dbSNP Id: rs121913014

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70884029G>A , CM000672.2:g.70884029G>A GRCh38
NC_000010.10:g.72643786G>A , CM000672.1:g.72643786G>A GRCh37
NC_000010.9:g.72313792G>A NCBI36
NG_008646.1:g.9756C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000697988.1:c.571-9730G>A (SGPL1) ENSP00000513492.1:n.571-9730G>A
ENST00000299299.4:c.236C>T (PCBD1) MANE Select ENSP00000299299.3:p.Thr79Ile
ENST00000299299.3:c.236C>T (PCBD1) ENSP00000299299.3:p.Thr79Ile
ENST00000493228.1:n.635C>T (PCBD1)
ENST00000493961.5:n.183+1123C>T (PCBD1)
NM_000281.3:c.236C>T (PCBD1) NP_000272.1:p.Thr79Ile
NM_001289797.1:c.89C>T (PCBD1) NP_001276726.1:p.Thr30Ile
XM_005269877.1:c.216+1123C>T (PCBD1) XP_005269934.1:n.216+1123C>T
NM_001323004.1:c.216+1123C>T (PCBD1) NP_001309933.1:n.216+1123C>T
NM_000281.4:c.236C>T (PCBD1) MANE Select NP_000272.1:p.Thr79Ile
NM_001289797.2:c.89C>T (PCBD1) NP_001276726.1:p.Thr30Ile
NM_001323004.2:c.216+1123C>T (PCBD1) NP_001309933.1:n.216+1123C>T