Canonical Allele Identifier: CA475501290

Gene: PC

Linked Data

• dbSNP Id: rs1276612567
• gnomAD v4: 11-66850156-CAAG-C
• MyVariant Identifiers: chr11:g.66617628_66617630del (hg19) ; chr11:g.66850157_66850159del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66850157_66850159del , CM000673.2:g.66850157_66850159del	GRCh38
NC_000011.9:g.66617628_66617630del , CM000673.1:g.66617628_66617630del	GRCh37
NC_000011.8:g.66374204_66374206del	NCBI36
NG_008319.1:g.113218_113220del

Transcript Alleles

HGVS	Amino-acid change
ENST00000393958.7:c.2719-43_2719-41del	ENSP00000377530.2:n.2719-43_2719-41del
ENST00000393960.7:c.2719-43_2719-41del MANE Select	ENSP00000377532.1:n.2719-43_2719-41del
ENST00000525476.2:n.290-94_290-92del
ENST00000528224.2:c.*728-43_*728-41del	ENSP00000498317.1:n.*728-43_*728-41del
ENST00000529047.6:c.2719-43_2719-41del	ENSP00000435905.2:n.2719-43_2719-41del
ENST00000651036.1:c.2719-43_2719-41del	ENSP00000498406.1:n.2719-43_2719-41del
ENST00000651469.1:c.*1195-43_*1195-41del	ENSP00000498712.1:n.*1195-43_*1195-41del
ENST00000651854.1:c.2719-43_2719-41del	ENSP00000498994.1:n.2719-43_2719-41del
ENST00000652125.1:c.2719-43_2719-41del	ENSP00000498302.1:n.2719-43_2719-41del
ENST00000393955.6:c.2719-43_2719-41del	ENSP00000377527.2:n.2719-43_2719-41del
ENST00000393958.6:c.2719-43_2719-41del	ENSP00000377530.2:n.2719-43_2719-41del
ENST00000393960.5:c.2719-43_2719-41del	ENSP00000377532.1:n.2719-43_2719-41del
ENST00000529047.5:c.79-43_79-41del	ENSP00000435905.1:n.79-43_79-41del
NM_000920.3:c.2719-43_2719-41del	NP_000911.2:n.2719-43_2719-41del
NM_001040716.1:c.2719-43_2719-41del	NP_001035806.1:n.2719-43_2719-41del
NM_022172.2:c.2719-43_2719-41del	NP_071504.2:n.2719-43_2719-41del
XM_005274031.3:c.2719-43_2719-41del	XP_005274088.1:n.2719-43_2719-41del
XM_005274032.3:c.2719-43_2719-41del	XP_005274089.1:n.2719-43_2719-41del
XM_006718577.2:c.2719-43_2719-41del	XP_006718640.1:n.2719-43_2719-41del
XM_006718578.2:c.2719-43_2719-41del	XP_006718641.1:n.2719-43_2719-41del
XM_006718579.2:c.1198-43_1198-41del	XP_006718642.1:n.1198-43_1198-41del
XM_011545085.1:c.2719-43_2719-41del	XP_011543387.1:n.2719-43_2719-41del
XM_011545086.1:c.2719-43_2719-41del	XP_011543388.1:n.2719-43_2719-41del
XM_011545087.1:c.1423-43_1423-41del	XP_011543389.1:n.1423-43_1423-41del
XM_011545088.1:c.1354-43_1354-41del	XP_011543390.1:n.1354-43_1354-41del
XM_005274031.4:c.2719-43_2719-41del	XP_005274088.1:n.2719-43_2719-41del
XM_005274032.4:c.2719-43_2719-41del	XP_005274089.1:n.2719-43_2719-41del
XM_006718578.3:c.2719-43_2719-41del	XP_006718641.1:n.2719-43_2719-41del
XM_006718579.3:c.1198-43_1198-41del	XP_006718642.1:n.1198-43_1198-41del
XM_011545086.2:c.2719-43_2719-41del	XP_011543388.1:n.2719-43_2719-41del
XM_011545087.2:c.1423-43_1423-41del	XP_011543389.1:n.1423-43_1423-41del
XM_017017868.1:c.2719-43_2719-41del	XP_016873357.1:n.2719-43_2719-41del
XM_017017869.1:c.2719-43_2719-41del	XP_016873358.1:n.2719-43_2719-41del
XM_017017870.1:c.2719-43_2719-41del	XP_016873359.1:n.2719-43_2719-41del
XM_017017871.1:c.2719-43_2719-41del	XP_016873360.1:n.2719-43_2719-41del
XM_017017872.2:c.2719-43_2719-41del	XP_016873361.1:n.2719-43_2719-41del
NM_000920.4:c.2719-43_2719-41del	NP_000911.2:n.2719-43_2719-41del
NM_001040716.2:c.2719-43_2719-41del MANE Select	NP_001035806.1:n.2719-43_2719-41del
NM_022172.3:c.2719-43_2719-41del	NP_071504.2:n.2719-43_2719-41del