Canonical Allele Identifier: CA381492594

Gene: PC

Linked Data

• ClinVar Variation Id: 1315510
• ClinVar RCV Id: RCV001774758
• dbSNP Id: rs1555015018
• MyVariant Identifiers: chr11:g.66617803C>G (hg19) ; chr11:g.66850332C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66850332C>G , CM000673.2:g.66850332C>G	GRCh38
NC_000011.9:g.66617803C>G , CM000673.1:g.66617803C>G	GRCh37
NC_000011.8:g.66374379C>G	NCBI36
NG_008319.1:g.113045G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393958.7:c.2606G>C	ENSP00000377530.2:p.Gly869Ala
ENST00000393960.7:c.2606G>C MANE Select	ENSP00000377532.1:p.Gly869Ala
ENST00000525476.2:n.290-267G>C
ENST00000528224.2:c.*615G>C	ENSP00000498317.1:n.*615G>C
ENST00000529047.6:c.2606G>C	ENSP00000435905.2:p.Gly869Ala
ENST00000651036.1:c.2606G>C	ENSP00000498406.1:p.Gly869Ala
ENST00000651469.1:c.*1082G>C	ENSP00000498712.1:n.*1082G>C
ENST00000651854.1:c.2606G>C	ENSP00000498994.1:p.Gly869Ala
ENST00000652125.1:c.2606G>C	ENSP00000498302.1:p.Gly869Ala
ENST00000393955.6:c.2606G>C	ENSP00000377527.2:p.Gly869Ala
ENST00000393958.6:c.2606G>C	ENSP00000377530.2:p.Gly869Ala
ENST00000393960.5:c.2606G>C	ENSP00000377532.1:p.Gly869Ala
ENST00000529047.5:c.-35G>C	ENSP00000435905.1:n.-35G>C
NM_000920.3:c.2606G>C	NP_000911.2:p.Gly869Ala
NM_001040716.1:c.2606G>C	NP_001035806.1:p.Gly869Ala
NM_022172.2:c.2606G>C	NP_071504.2:p.Gly869Ala
XM_005274031.3:c.2606G>C	XP_005274088.1:p.Gly869Ala
XM_005274032.3:c.2606G>C	XP_005274089.1:p.Gly869Ala
XM_006718577.2:c.2606G>C	XP_006718640.1:p.Gly869Ala
XM_006718578.2:c.2606G>C	XP_006718641.1:p.Gly869Ala
XM_006718579.2:c.1085G>C	XP_006718642.1:p.Gly362Ala
XM_011545085.1:c.2606G>C	XP_011543387.1:p.Gly869Ala
XM_011545086.1:c.2606G>C	XP_011543388.1:p.Gly869Ala
XM_011545087.1:c.1310G>C	XP_011543389.1:p.Gly437Ala
XM_011545088.1:c.1241G>C	XP_011543390.1:p.Gly414Ala
XM_005274031.4:c.2606G>C	XP_005274088.1:p.Gly869Ala
XM_005274032.4:c.2606G>C	XP_005274089.1:p.Gly869Ala
XM_006718578.3:c.2606G>C	XP_006718641.1:p.Gly869Ala
XM_006718579.3:c.1085G>C	XP_006718642.1:p.Gly362Ala
XM_011545086.2:c.2606G>C	XP_011543388.1:p.Gly869Ala
XM_011545087.2:c.1310G>C	XP_011543389.1:p.Gly437Ala
XM_017017868.1:c.2606G>C	XP_016873357.1:p.Gly869Ala
XM_017017869.1:c.2606G>C	XP_016873358.1:p.Gly869Ala
XM_017017870.1:c.2606G>C	XP_016873359.1:p.Gly869Ala
XM_017017871.1:c.2606G>C	XP_016873360.1:p.Gly869Ala
XM_017017872.2:c.2606G>C	XP_016873361.1:p.Gly869Ala
NM_000920.4:c.2606G>C	NP_000911.2:p.Gly869Ala
NM_001040716.2:c.2606G>C MANE Select	NP_001035806.1:p.Gly869Ala
NM_022172.3:c.2606G>C	NP_071504.2:p.Gly869Ala