Canonical Allele Identifier: CA368020212

Gene: PCLO

Linked Data

• MyVariant Identifiers: chr7:g.82453627G>A (hg19) ; chr7:g.82824311G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824311G>A , CM000669.2:g.82824311G>A	GRCh38
NC_000007.13:g.82453627G>A , CM000669.1:g.82453627G>A	GRCh37
NC_000007.12:g.82291563G>A	NCBI36
NG_047145.1:g.343571C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000333891.14:c.14521C>T MANE Select	ENSP00000334319.8:p.Gln4841Ter
ENST00000333891.13:c.14521C>T	ENSP00000334319.8:p.Gln4841Ter
ENST00000423517.6:c.14521C>T	ENSP00000388393.2:p.Gln4841Ter
ENST00000426442.6:n.1016C>T
ENST00000618073.1:c.784C>T	ENSP00000482390.1:p.Gln262Ter
NM_014510.2:c.14521C>T	NP_055325.2:p.Gln4841Ter
NM_033026.5:c.14521C>T	NP_149015.2:p.Gln4841Ter
XM_017012006.2:c.7426C>T	XP_016867495.1:p.Gln2476Ter
XM_017012007.1:c.7399C>T	XP_016867496.1:p.Gln2467Ter
XR_001744643.2:n.16090C>T
NM_033026.6:c.14521C>T MANE Select	NP_149015.2:p.Gln4841Ter
NM_014510.3:c.14521C>T	NP_055325.2:p.Gln4841Ter