Canonical Allele Identifier: CA470052903

Gene: SGPL1 PCBD1

Linked Data

• MyVariant Identifiers: chr10:g.72643719C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70883962C>A , CM000672.2:g.70883962C>A	GRCh38
NC_000010.10:g.72643719C>A , CM000672.1:g.72643719C>A	GRCh37
NC_000010.9:g.72313725C>A	NCBI36
NG_008646.1:g.9823G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697988.1:c.571-9797C>A (SGPL1)	ENSP00000513492.1:n.571-9797C>A
ENST00000299299.4:c.303G>T (PCBD1) MANE Select	ENSP00000299299.3:p.Val101=
ENST00000299299.3:c.303G>T (PCBD1)	ENSP00000299299.3:p.Val101=
ENST00000493228.1:n.702G>T (PCBD1)
ENST00000493961.5:n.183+1190G>T (PCBD1)
NM_000281.3:c.303G>T (PCBD1)	NP_000272.1:p.Val101=
NM_001289797.1:c.156G>T (PCBD1)	NP_001276726.1:p.Val52=
XM_005269877.1:c.216+1190G>T (PCBD1)	XP_005269934.1:n.216+1190G>T
NM_001323004.1:c.216+1190G>T (PCBD1)	NP_001309933.1:n.216+1190G>T
NM_000281.4:c.303G>T (PCBD1) MANE Select	NP_000272.1:p.Val101=
NM_001289797.2:c.156G>T (PCBD1)	NP_001276726.1:p.Val52=
NM_001323004.2:c.216+1190G>T (PCBD1)	NP_001309933.1:n.216+1190G>T