Canonical Allele Identifier: CA679449368

Gene: PC

Linked Data

• dbSNP Id: rs1312106266
• gnomAD v3: 11-66871263-G-A
• gnomAD v4: 11-66871263-G-A
• MyVariant Identifiers: chr11:g.66638734G>A (hg19) ; chr11:g.66871263G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66871263G>A , CM000673.2:g.66871263G>A	GRCh38
NC_000011.9:g.66638734G>A , CM000673.1:g.66638734G>A	GRCh37
NC_000011.8:g.66395310G>A	NCBI36
NG_008319.1:g.92114C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000393958.7:c.487+52C>T	ENSP00000377530.2:n.487+52C>T
ENST00000393960.7:c.487+52C>T MANE Select	ENSP00000377532.1:n.487+52C>T
ENST00000524491.6:c.487+52C>T	ENSP00000434192.2:n.487+52C>T
ENST00000525476.2:n.290-21198C>T
ENST00000528224.2:c.487+52C>T	ENSP00000498317.1:n.487+52C>T
ENST00000528403.6:c.487+52C>T	ENSP00000498816.1:n.487+52C>T
ENST00000529047.6:c.487+52C>T	ENSP00000435905.2:n.487+52C>T
ENST00000651036.1:c.487+52C>T	ENSP00000498406.1:n.487+52C>T
ENST00000651469.1:c.487+52C>T	ENSP00000498712.1:n.487+52C>T
ENST00000651854.1:c.487+52C>T	ENSP00000498994.1:n.487+52C>T
ENST00000652125.1:c.487+52C>T	ENSP00000498302.1:n.487+52C>T
ENST00000393955.6:c.487+52C>T	ENSP00000377527.2:n.487+52C>T
ENST00000393958.6:c.487+52C>T	ENSP00000377530.2:n.487+52C>T
ENST00000393960.5:c.487+52C>T	ENSP00000377532.1:n.487+52C>T
ENST00000524491.5:c.367+52C>T	ENSP00000434192.1:n.367+52C>T
ENST00000628663.1:c.367+52C>T	ENSP00000486373.1:n.367+52C>T
NM_000920.3:c.487+52C>T	NP_000911.2:n.487+52C>T
NM_001040716.1:c.487+52C>T	NP_001035806.1:n.487+52C>T
NM_022172.2:c.487+52C>T	NP_071504.2:n.487+52C>T
XM_005274031.3:c.487+52C>T	XP_005274088.1:n.487+52C>T
XM_005274032.3:c.487+52C>T	XP_005274089.1:n.487+52C>T
XM_006718577.2:c.487+52C>T	XP_006718640.1:n.487+52C>T
XM_006718578.2:c.487+52C>T	XP_006718641.1:n.487+52C>T
XM_011545085.1:c.487+52C>T	XP_011543387.1:n.487+52C>T
XM_011545086.1:c.487+52C>T	XP_011543388.1:n.487+52C>T
XM_005274031.4:c.487+52C>T	XP_005274088.1:n.487+52C>T
XM_005274032.4:c.487+52C>T	XP_005274089.1:n.487+52C>T
XM_006718578.3:c.487+52C>T	XP_006718641.1:n.487+52C>T
XM_011545086.2:c.487+52C>T	XP_011543388.1:n.487+52C>T
XM_017017868.1:c.487+52C>T	XP_016873357.1:n.487+52C>T
XM_017017869.1:c.487+52C>T	XP_016873358.1:n.487+52C>T
XM_017017870.1:c.487+52C>T	XP_016873359.1:n.487+52C>T
XM_017017871.1:c.487+52C>T	XP_016873360.1:n.487+52C>T
XM_017017872.2:c.487+52C>T	XP_016873361.1:n.487+52C>T
NM_000920.4:c.487+52C>T	NP_000911.2:n.487+52C>T
NM_001040716.2:c.487+52C>T MANE Select	NP_001035806.1:n.487+52C>T
NM_022172.3:c.487+52C>T	NP_071504.2:n.487+52C>T