Canonical Allele Identifier: CA717052952

Gene: PRC1

Linked Data

• dbSNP Id: rs1344934627
• gnomAD v3: 15-90966303-C-G
• gnomAD v4: 15-90966303-C-G
• MyVariant Identifiers: chr15:g.91509533C>G (hg19) ; chr15:g.90966303C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966303C>G , CM000677.2:g.90966303C>G	GRCh38
NC_000015.9:g.91509533C>G , CM000677.1:g.91509533C>G	GRCh37
NC_000015.8:g.89310537C>G	NCBI36
NG_050647.1:g.33349G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*828G>C MANE Select	ENSP00000377793.3:n.*828G>C
ENST00000643536.1:c.*4453G>C	ENSP00000494429.1:n.*4453G>C
ENST00000361188.9:c.*828G>C	ENSP00000354679.5:n.*828G>C
ENST00000394249.7:c.*828G>C	ENSP00000377793.3:n.*828G>C
ENST00000556972.6:c.475G>C	ENSP00000456737.1:n.475G>C
NM_001267580.1:c.*871G>C	NP_001254509.1:n.*871G>C
NM_003981.3:c.*828G>C	NP_003972.1:n.*828G>C
NM_199413.2:c.*828G>C	NP_955445.1:n.*828G>C
XM_005254987.1:c.*871G>C	XP_005255044.1:n.*871G>C
XM_006720759.1:c.*922G>C	XP_006720822.1:n.*922G>C
XM_006720760.1:c.*334G>C	XP_006720823.1:n.*334G>C
XM_011522187.1:c.*276G>C	XP_011520489.1:n.*276G>C
XM_011522188.1:c.*276G>C	XP_011520490.1:n.*276G>C
XM_011522189.1:c.*276G>C	XP_011520491.1:n.*276G>C
XM_011522190.1:c.*276G>C	XP_011520492.1:n.*276G>C
XM_011522192.1:c.*276G>C	XP_011520494.1:n.*276G>C
XM_005254987.3:c.*871G>C	XP_005255044.1:n.*871G>C
XM_006720759.2:c.*922G>C	XP_006720822.1:n.*922G>C
XM_006720760.2:c.*334G>C	XP_006720823.1:n.*334G>C
XM_011522187.2:c.*276G>C	XP_011520489.1:n.*276G>C
XM_011522188.3:c.*276G>C	XP_011520490.1:n.*276G>C
XM_011522189.2:c.*276G>C	XP_011520491.1:n.*276G>C
XM_011522191.3:c.*373G>C	XP_011520493.1:n.*373G>C
XM_011522192.2:c.*276G>C	XP_011520494.1:n.*276G>C
XM_017022712.2:c.*828G>C	XP_016878201.1:n.*828G>C
XM_017022713.2:c.*828G>C	XP_016878202.1:n.*828G>C
XM_017022715.2:c.*828G>C	XP_016878204.1:n.*828G>C
XM_017022716.2:c.*828G>C	XP_016878205.1:n.*828G>C
XM_017022717.1:c.*871G>C	XP_016878206.1:n.*871G>C
NM_003981.4:c.*828G>C MANE Select	NP_003972.2:n.*828G>C
NM_001267580.2:c.*871G>C	NP_001254509.2:n.*871G>C
NM_199413.3:c.*828G>C	NP_955445.2:n.*828G>C