Canonical Allele Identifier: CA368020198

Gene: PCLO

Linked Data

• dbSNP Id: rs1467947402
• gnomAD v3: 7-82824308-T-G
• gnomAD v4: 7-82824308-T-G
• MyVariant Identifiers: chr7:g.82453624T>G (hg19) ; chr7:g.82824308T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824308T>G , CM000669.2:g.82824308T>G	GRCh38
NC_000007.13:g.82453624T>G , CM000669.1:g.82453624T>G	GRCh37
NC_000007.12:g.82291560T>G	NCBI36
NG_047145.1:g.343574A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000333891.14:c.14524A>C MANE Select	ENSP00000334319.8:p.Ser4842Arg
ENST00000333891.13:c.14524A>C	ENSP00000334319.8:p.Ser4842Arg
ENST00000423517.6:c.14524A>C	ENSP00000388393.2:p.Ser4842Arg
ENST00000426442.6:n.1019A>C
ENST00000618073.1:c.787A>C	ENSP00000482390.1:p.Ser263Arg
NM_014510.2:c.14524A>C	NP_055325.2:p.Ser4842Arg
NM_033026.5:c.14524A>C	NP_149015.2:p.Ser4842Arg
XM_017012006.2:c.7429A>C	XP_016867495.1:p.Ser2477Arg
XM_017012007.1:c.7402A>C	XP_016867496.1:p.Ser2468Arg
XR_001744643.2:n.16093A>C
NM_033026.6:c.14524A>C MANE Select	NP_149015.2:p.Ser4842Arg
NM_014510.3:c.14524A>C	NP_055325.2:p.Ser4842Arg