Canonical Allele Identifier: CA2630414192

Gene: PRC1

Linked Data

• gnomAD v4: 15-90966353-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966353C>G , CM000677.2:g.90966353C>G	GRCh38
NC_000015.9:g.91509583C>G , CM000677.1:g.91509583C>G	GRCh37
NC_000015.8:g.89310587C>G	NCBI36
NG_050647.1:g.33299G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*778G>C MANE Select	ENSP00000377793.3:n.*778G>C
ENST00000643536.1:c.*4403G>C	ENSP00000494429.1:n.*4403G>C
ENST00000361188.9:c.*778G>C	ENSP00000354679.5:n.*778G>C
ENST00000394249.7:c.*778G>C	ENSP00000377793.3:n.*778G>C
ENST00000556972.6:c.425G>C	ENSP00000456737.1:n.425G>C
NM_001267580.1:c.*821G>C	NP_001254509.1:n.*821G>C
NM_003981.3:c.*778G>C	NP_003972.1:n.*778G>C
NM_199413.2:c.*778G>C	NP_955445.1:n.*778G>C
XM_005254987.1:c.*821G>C	XP_005255044.1:n.*821G>C
XM_006720759.1:c.*872G>C	XP_006720822.1:n.*872G>C
XM_006720760.1:c.*284G>C	XP_006720823.1:n.*284G>C
XM_011522187.1:c.*226G>C	XP_011520489.1:n.*226G>C
XM_011522188.1:c.*226G>C	XP_011520490.1:n.*226G>C
XM_011522189.1:c.*226G>C	XP_011520491.1:n.*226G>C
XM_011522190.1:c.*226G>C	XP_011520492.1:n.*226G>C
XM_011522192.1:c.*226G>C	XP_011520494.1:n.*226G>C
XM_005254987.3:c.*821G>C	XP_005255044.1:n.*821G>C
XM_006720759.2:c.*872G>C	XP_006720822.1:n.*872G>C
XM_006720760.2:c.*284G>C	XP_006720823.1:n.*284G>C
XM_011522187.2:c.*226G>C	XP_011520489.1:n.*226G>C
XM_011522188.3:c.*226G>C	XP_011520490.1:n.*226G>C
XM_011522189.2:c.*226G>C	XP_011520491.1:n.*226G>C
XM_011522191.3:c.*323G>C	XP_011520493.1:n.*323G>C
XM_011522192.2:c.*226G>C	XP_011520494.1:n.*226G>C
XM_017022712.2:c.*778G>C	XP_016878201.1:n.*778G>C
XM_017022713.2:c.*778G>C	XP_016878202.1:n.*778G>C
XM_017022715.2:c.*778G>C	XP_016878204.1:n.*778G>C
XM_017022716.2:c.*778G>C	XP_016878205.1:n.*778G>C
XM_017022717.1:c.*821G>C	XP_016878206.1:n.*821G>C
NM_003981.4:c.*778G>C MANE Select	NP_003972.2:n.*778G>C
NM_001267580.2:c.*821G>C	NP_001254509.2:n.*821G>C
NM_199413.3:c.*778G>C	NP_955445.2:n.*778G>C