Canonical Allele Identifier: CA1979908391

Gene: PC

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66895260G>C , CM000673.2:g.66895260G>C	GRCh38
NC_000011.9:g.66662731G>C , CM000673.1:g.66662731G>C	GRCh37
NC_000011.8:g.66419307G>C	NCBI36
NG_008319.1:g.68117C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393958.7:c.1-23101C>G	ENSP00000377530.2:n.1-23101C>G
ENST00000393960.7:c.1-23101C>G MANE Select	ENSP00000377532.1:n.1-23101C>G
ENST00000524491.6:c.1-23101C>G	ENSP00000434192.2:n.1-23101C>G
ENST00000525476.2:n.290-45195C>G
ENST00000528224.2:c.1-23101C>G	ENSP00000498317.1:n.1-23101C>G
ENST00000528403.6:c.1-23101C>G	ENSP00000498816.1:n.1-23101C>G
ENST00000529047.6:c.1-23101C>G	ENSP00000435905.2:n.1-23101C>G
ENST00000531614.6:c.1-23101C>G	ENSP00000498218.1:n.1-23101C>G
ENST00000651036.1:c.1-23101C>G	ENSP00000498406.1:n.1-23101C>G
ENST00000651469.1:c.1-23101C>G	ENSP00000498712.1:n.1-23101C>G
ENST00000651854.1:c.1-23101C>G	ENSP00000498994.1:n.1-23101C>G
ENST00000652125.1:c.1-23101C>G	ENSP00000498302.1:n.1-23101C>G
ENST00000393955.6:c.-1+12561C>G	ENSP00000377527.2:n.-1+12561C>G
ENST00000393958.6:c.1-23101C>G	ENSP00000377530.2:n.1-23101C>G
ENST00000393960.5:c.1-23101C>G	ENSP00000377532.1:n.1-23101C>G
ENST00000524491.5:c.-120-23101C>G	ENSP00000434192.1:n.-120-23101C>G
ENST00000528403.5:n.277-23101C>G
ENST00000531614.5:n.203-23101C>G
NM_000920.3:c.1-23101C>G	NP_000911.2:n.1-23101C>G
NM_001040716.1:c.1-23101C>G	NP_001035806.1:n.1-23101C>G
NM_022172.2:c.-1+12561C>G	NP_071504.2:n.-1+12561C>G
XM_006718577.2:c.1-23101C>G	XP_006718640.1:n.1-23101C>G
XM_006718578.2:c.1-23101C>G	XP_006718641.1:n.1-23101C>G
XM_011545085.1:c.-1+11062C>G	XP_011543387.1:n.-1+11062C>G
XM_011545086.1:c.-1+10628C>G	XP_011543388.1:n.-1+10628C>G
XM_006718578.3:c.1-23101C>G	XP_006718641.1:n.1-23101C>G
XM_011545086.2:c.-1+10628C>G	XP_011543388.1:n.-1+10628C>G
XM_017017868.1:c.1-23101C>G	XP_016873357.1:n.1-23101C>G
XM_017017869.1:c.1-23101C>G	XP_016873358.1:n.1-23101C>G
XM_017017870.1:c.1-23101C>G	XP_016873359.1:n.1-23101C>G
XM_017017871.1:c.1-23101C>G	XP_016873360.1:n.1-23101C>G
XM_017017872.2:c.-1+11062C>G	XP_016873361.1:n.-1+11062C>G
NM_000920.4:c.1-23101C>G	NP_000911.2:n.1-23101C>G
NM_001040716.2:c.1-23101C>G MANE Select	NP_001035806.1:n.1-23101C>G
NM_022172.3:c.-1+12561C>G	NP_071504.2:n.-1+12561C>G