Canonical Allele Identifier: CA341765
Gene: PC HGNC NCBI

Linked Data

dbSNP Id: rs113994147
MyVariant Identifiers: chr11:g.66617869G>A (hg19) chr11:g.66850398G>A (hg38)
PubMed: PMID:20301301 PMID:20301764
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66850398G>A , CM000673.2:g.66850398G>A GRCh38
NC_000011.9:g.66617869G>A , CM000673.1:g.66617869G>A GRCh37
NC_000011.8:g.66374445G>A NCBI36
NG_008319.1:g.112979C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000393958.7:c.2540C>T ENSP00000377530.2:p.Ala847Val
ENST00000393960.7:c.2540C>T MANE Select ENSP00000377532.1:p.Ala847Val
ENST00000525476.2:n.290-333C>T
ENST00000528224.2:c.*549C>T ENSP00000498317.1:n.*549C>T
ENST00000529047.6:c.2540C>T ENSP00000435905.2:p.Ala847Val
ENST00000651036.1:c.2540C>T ENSP00000498406.1:p.Ala847Val
ENST00000651469.1:c.*1016C>T ENSP00000498712.1:n.*1016C>T
ENST00000651854.1:c.2540C>T ENSP00000498994.1:p.Ala847Val
ENST00000652125.1:c.2540C>T ENSP00000498302.1:p.Ala847Val
ENST00000393955.6:c.2540C>T ENSP00000377527.2:p.Ala847Val
ENST00000393958.6:c.2540C>T ENSP00000377530.2:p.Ala847Val
ENST00000393960.5:c.2540C>T ENSP00000377532.1:p.Ala847Val
NM_000920.3:c.2540C>T NP_000911.2:p.Ala847Val
NM_001040716.1:c.2540C>T NP_001035806.1:p.Ala847Val
NM_022172.2:c.2540C>T NP_071504.2:p.Ala847Val
XM_005274031.3:c.2540C>T XP_005274088.1:p.Ala847Val
XM_005274032.3:c.2540C>T XP_005274089.1:p.Ala847Val
XM_006718577.2:c.2540C>T XP_006718640.1:p.Ala847Val
XM_006718578.2:c.2540C>T XP_006718641.1:p.Ala847Val
XM_006718579.2:c.1019C>T XP_006718642.1:p.Ala340Val
XM_011545085.1:c.2540C>T XP_011543387.1:p.Ala847Val
XM_011545086.1:c.2540C>T XP_011543388.1:p.Ala847Val
XM_011545087.1:c.1244C>T XP_011543389.1:p.Ala415Val
XM_011545088.1:c.1175C>T XP_011543390.1:p.Ala392Val
XM_005274031.4:c.2540C>T XP_005274088.1:p.Ala847Val
XM_005274032.4:c.2540C>T XP_005274089.1:p.Ala847Val
XM_006718578.3:c.2540C>T XP_006718641.1:p.Ala847Val
XM_006718579.3:c.1019C>T XP_006718642.1:p.Ala340Val
XM_011545086.2:c.2540C>T XP_011543388.1:p.Ala847Val
XM_011545087.2:c.1244C>T XP_011543389.1:p.Ala415Val
XM_017017868.1:c.2540C>T XP_016873357.1:p.Ala847Val
XM_017017869.1:c.2540C>T XP_016873358.1:p.Ala847Val
XM_017017870.1:c.2540C>T XP_016873359.1:p.Ala847Val
XM_017017871.1:c.2540C>T XP_016873360.1:p.Ala847Val
XM_017017872.2:c.2540C>T XP_016873361.1:p.Ala847Val
NM_000920.4:c.2540C>T NP_000911.2:p.Ala847Val
NM_001040716.2:c.2540C>T MANE Select NP_001035806.1:p.Ala847Val
NM_022172.3:c.2540C>T NP_071504.2:p.Ala847Val
Search 100 bp 5'
Search 100 bp 3'