Canonical Allele Identifier: CA2630413669

Gene: PRC1

Linked Data

• gnomAD v4: 15-90966194-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966194A>G , CM000677.2:g.90966194A>G	GRCh38
NC_000015.9:g.91509424A>G , CM000677.1:g.91509424A>G	GRCh37
NC_000015.8:g.89310428A>G	NCBI36
NG_050647.1:g.33458T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*937T>C MANE Select	ENSP00000377793.3:n.*937T>C
ENST00000643536.1:c.*4562T>C	ENSP00000494429.1:n.*4562T>C
ENST00000361188.9:c.*937T>C	ENSP00000354679.5:n.*937T>C
ENST00000394249.7:c.*937T>C	ENSP00000377793.3:n.*937T>C
ENST00000556972.6:c.584T>C	ENSP00000456737.1:n.584T>C
NM_001267580.1:c.*980T>C	NP_001254509.1:n.*980T>C
NM_003981.3:c.*937T>C	NP_003972.1:n.*937T>C
NM_199413.2:c.*937T>C	NP_955445.1:n.*937T>C
XM_005254987.1:c.*980T>C	XP_005255044.1:n.*980T>C
XM_006720759.1:c.*1031T>C	XP_006720822.1:n.*1031T>C
XM_006720760.1:c.*443T>C	XP_006720823.1:n.*443T>C
XM_011522187.1:c.*385T>C	XP_011520489.1:n.*385T>C
XM_011522188.1:c.*385T>C	XP_011520490.1:n.*385T>C
XM_011522189.1:c.*385T>C	XP_011520491.1:n.*385T>C
XM_011522190.1:c.*385T>C	XP_011520492.1:n.*385T>C
XM_011522192.1:c.*385T>C	XP_011520494.1:n.*385T>C
XM_005254987.3:c.*980T>C	XP_005255044.1:n.*980T>C
XM_006720759.2:c.*1031T>C	XP_006720822.1:n.*1031T>C
XM_006720760.2:c.*443T>C	XP_006720823.1:n.*443T>C
XM_011522187.2:c.*385T>C	XP_011520489.1:n.*385T>C
XM_011522188.3:c.*385T>C	XP_011520490.1:n.*385T>C
XM_011522189.2:c.*385T>C	XP_011520491.1:n.*385T>C
XM_011522191.3:c.*482T>C	XP_011520493.1:n.*482T>C
XM_011522192.2:c.*385T>C	XP_011520494.1:n.*385T>C
XM_017022712.2:c.*937T>C	XP_016878201.1:n.*937T>C
XM_017022713.2:c.*937T>C	XP_016878202.1:n.*937T>C
XM_017022715.2:c.*937T>C	XP_016878204.1:n.*937T>C
XM_017022716.2:c.*937T>C	XP_016878205.1:n.*937T>C
XM_017022717.1:c.*980T>C	XP_016878206.1:n.*980T>C
NM_003981.4:c.*937T>C MANE Select	NP_003972.2:n.*937T>C
NM_001267580.2:c.*980T>C	NP_001254509.2:n.*980T>C
NM_199413.3:c.*937T>C	NP_955445.2:n.*937T>C