Canonical Allele Identifier: CA381496695

Gene: PC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66853380T>C , CM000673.2:g.66853380T>C	GRCh38
NC_000011.9:g.66620851T>C , CM000673.1:g.66620851T>C	GRCh37
NC_000011.8:g.66377427T>C	NCBI36
NG_008319.1:g.109997A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001040716.2:c.1372A>G MANE Select	NP_001035806.1:p.Asn458Asp
ENST00000393960.7:c.1372A>G MANE Select	ENSP00000377532.1:p.Asn458Asp
NM_000920.3:c.1372A>G	NP_000911.2:p.Asn458Asp
NM_000920.4:c.1372A>G	NP_000911.2:p.Asn458Asp
NM_001040716.1:c.1372A>G	NP_001035806.1:p.Asn458Asp
NM_022172.2:c.1372A>G	NP_071504.2:p.Asn458Asp
NM_022172.3:c.1372A>G	NP_071504.2:p.Asn458Asp
ENST00000393955.6:c.1372A>G	ENSP00000377527.2:p.Asn458Asp
ENST00000393958.6:c.1372A>G	ENSP00000377530.2:p.Asn458Asp
ENST00000393958.7:c.1372A>G	ENSP00000377530.2:p.Asn458Asp
ENST00000393960.5:c.1372A>G	ENSP00000377532.1:p.Asn458Asp
ENST00000525476.2:n.290-3315A>G
ENST00000528224.2:c.1372A>G	ENSP00000498317.1:p.Asn458Asp
ENST00000528403.6:c.1372A>G	ENSP00000498816.1:p.Asn458Asp
ENST00000529047.6:c.1372A>G	ENSP00000435905.2:p.Asn458Asp
ENST00000651036.1:c.1372A>G	ENSP00000498406.1:p.Asn458Asp
ENST00000651469.1:c.1440A>G	ENSP00000498712.1:p.Pro480=
ENST00000651831.1:n.198A>G
ENST00000651854.1:c.1372A>G	ENSP00000498994.1:p.Asn458Asp
ENST00000652125.1:c.1372A>G	ENSP00000498302.1:p.Asn458Asp
ENST00000652387.1:n.235A>G
XM_005274031.3:c.1372A>G	XP_005274088.1:p.Asn458Asp
XM_005274031.4:c.1372A>G	XP_005274088.1:p.Asn458Asp
XM_005274032.3:c.1372A>G	XP_005274089.1:p.Asn458Asp
XM_005274032.4:c.1372A>G	XP_005274089.1:p.Asn458Asp
XM_006718577.2:c.1372A>G	XP_006718640.1:p.Asn458Asp
XM_006718578.2:c.1372A>G	XP_006718641.1:p.Asn458Asp
XM_006718578.3:c.1372A>G	XP_006718641.1:p.Asn458Asp
XM_006718579.2:c.-150A>G	XP_006718642.1:n.-150A>G
XM_006718579.3:c.-150A>G	XP_006718642.1:n.-150A>G
XM_011545085.1:c.1372A>G	XP_011543387.1:p.Asn458Asp
XM_011545086.1:c.1372A>G	XP_011543388.1:p.Asn458Asp
XM_011545086.2:c.1372A>G	XP_011543388.1:p.Asn458Asp
XM_011545087.1:c.76A>G	XP_011543389.1:p.Asn26Asp
XM_011545087.2:c.76A>G	XP_011543389.1:p.Asn26Asp
XM_011545088.1:c.7A>G	XP_011543390.1:p.Asn3Asp
XM_017017868.1:c.1372A>G	XP_016873357.1:p.Asn458Asp
XM_017017869.1:c.1372A>G	XP_016873358.1:p.Asn458Asp
XM_017017870.1:c.1372A>G	XP_016873359.1:p.Asn458Asp
XM_017017871.1:c.1372A>G	XP_016873360.1:p.Asn458Asp
XM_017017872.2:c.1372A>G	XP_016873361.1:p.Asn458Asp