Canonical Allele Identifier: CA1918455759
Community Standard Title: NM_000281.4(PCBD1):c.236C= (p.Thr79=)

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_000281.4:c.236C= (PCBD1) MANE Select NP_000272.1:p.Thr79=
ENST00000299299.4:c.236C= (PCBD1) MANE Select ENSP00000299299.3:p.Thr79=
NM_000281.3:c.236C= (PCBD1) NP_000272.1:p.Thr79=
NM_001289797.1:c.89C= (PCBD1) NP_001276726.1:p.Thr30=
NM_001289797.2:c.89C= (PCBD1) NP_001276726.1:p.Thr30=
NM_001323004.1:c.216+1123C= (PCBD1) NP_001309933.1:n.216+1123C=
NM_001323004.2:c.216+1123C= (PCBD1) NP_001309933.1:n.216+1123C=
ENST00000299299.3:c.236C= (PCBD1) ENSP00000299299.3:p.Thr79=
ENST00000493228.1:n.635C= (PCBD1)
ENST00000493961.5:n.183+1123C= (PCBD1)
ENST00000697988.1:c.571-9730G= (SGPL1) ENSP00000513492.1:n.571-9730G=
XM_005269877.1:c.216+1123C= (PCBD1) XP_005269934.1:n.216+1123C=