Canonical Allele Identifier: CA368020202

Gene: PCLO

Linked Data

• MyVariant Identifiers: chr7:g.82453625C>A (hg19) ; chr7:g.82824309C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824309C>A , CM000669.2:g.82824309C>A	GRCh38
NC_000007.13:g.82453625C>A , CM000669.1:g.82453625C>A	GRCh37
NC_000007.12:g.82291561C>A	NCBI36
NG_047145.1:g.343573G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000333891.14:c.14523G>T MANE Select	ENSP00000334319.8:p.Gln4841His
ENST00000333891.13:c.14523G>T	ENSP00000334319.8:p.Gln4841His
ENST00000423517.6:c.14523G>T	ENSP00000388393.2:p.Gln4841His
ENST00000426442.6:n.1018G>T
ENST00000618073.1:c.786G>T	ENSP00000482390.1:p.Gln262His
NM_014510.2:c.14523G>T	NP_055325.2:p.Gln4841His
NM_033026.5:c.14523G>T	NP_149015.2:p.Gln4841His
XM_017012006.2:c.7428G>T	XP_016867495.1:p.Gln2476His
XM_017012007.1:c.7401G>T	XP_016867496.1:p.Gln2467His
XR_001744643.2:n.16092G>T
NM_033026.6:c.14523G>T MANE Select	NP_149015.2:p.Gln4841His
NM_014510.3:c.14523G>T	NP_055325.2:p.Gln4841His