Canonical Allele Identifier: CA10639842

Gene: PC

Linked Data

• ClinVar Variation Id: 305637
• ClinVar RCV Id: RCV000340170
• dbSNP Id: rs886048558
• gnomAD v2: 11-66725847-C-T
• gnomAD v3: 11-66958376-C-T
• gnomAD v4: 11-66958376-C-T
• MyVariant Identifiers: chr11:g.66725847C>T (hg19) ; chr11:g.66958376C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66958376C>T , CM000673.2:g.66958376C>T	GRCh38
NC_000011.9:g.66725847C>T , CM000673.1:g.66725847C>T	GRCh37
NC_000011.8:g.66482423C>T	NCBI36
NG_008319.1:g.5001G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000393958.7:c.-94G>A	ENSP00000377530.2:n.-94G>A
ENST00000393960.7:c.-282G>A MANE Select	ENSP00000377532.1:n.-282G>A
ENST00000524491.6:c.-94G>A	ENSP00000434192.2:n.-94G>A
ENST00000525476.2:n.8G>A
ENST00000528224.2:c.-94G>A	ENSP00000498317.1:n.-94G>A
ENST00000528403.6:c.-351G>A	ENSP00000498816.1:n.-351G>A
ENST00000529047.6:c.-222G>A	ENSP00000435905.2:n.-222G>A
ENST00000651854.1:c.-1241G>A	ENSP00000498994.1:n.-1241G>A
ENST00000393958.6:c.-94G>A	ENSP00000377530.2:n.-94G>A
ENST00000393960.5:c.-282G>A	ENSP00000377532.1:n.-282G>A
ENST00000524491.5:c.-214G>A	ENSP00000434192.1:n.-214G>A
NM_000920.3:c.-94G>A	NP_000911.2:n.-94G>A
NM_001040716.1:c.-282G>A	NP_001035806.1:n.-282G>A
XR_950230.1:n.87+4041C>T
XM_006718578.3:c.-55G>A	XP_006718641.1:n.-55G>A
XM_017017868.1:c.-539G>A	XP_016873357.1:n.-539G>A
XM_017017869.1:c.-410G>A	XP_016873358.1:n.-410G>A
XM_017017870.1:c.-351G>A	XP_016873359.1:n.-351G>A
XM_017017871.1:c.-222G>A	XP_016873360.1:n.-222G>A
XR_950230.2:n.87+4041C>T
NM_000920.4:c.-94G>A	NP_000911.2:n.-94G>A
NM_001040716.2:c.-282G>A MANE Select	NP_001035806.1:n.-282G>A