Canonical Allele Identifier: CA2739484595

Gene: PRC1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966225A>G , CM000677.2:g.90966225A>G	GRCh38
NC_000015.9:g.91509455A>G , CM000677.1:g.91509455A>G	GRCh37
NC_000015.8:g.89310459A>G	NCBI36
NG_050647.1:g.33427T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*906T>C MANE Select	ENSP00000377793.3:n.*906T>C
ENST00000643536.1:c.*4531T>C	ENSP00000494429.1:n.*4531T>C
ENST00000361188.9:c.*906T>C	ENSP00000354679.5:n.*906T>C
ENST00000394249.7:c.*906T>C	ENSP00000377793.3:n.*906T>C
ENST00000556972.6:c.553T>C	ENSP00000456737.1:n.553T>C
NM_001267580.1:c.*949T>C	NP_001254509.1:n.*949T>C
NM_003981.3:c.*906T>C	NP_003972.1:n.*906T>C
NM_199413.2:c.*906T>C	NP_955445.1:n.*906T>C
XM_005254987.1:c.*949T>C	XP_005255044.1:n.*949T>C
XM_006720759.1:c.*1000T>C	XP_006720822.1:n.*1000T>C
XM_006720760.1:c.*412T>C	XP_006720823.1:n.*412T>C
XM_011522187.1:c.*354T>C	XP_011520489.1:n.*354T>C
XM_011522188.1:c.*354T>C	XP_011520490.1:n.*354T>C
XM_011522189.1:c.*354T>C	XP_011520491.1:n.*354T>C
XM_011522190.1:c.*354T>C	XP_011520492.1:n.*354T>C
XM_011522192.1:c.*354T>C	XP_011520494.1:n.*354T>C
XM_005254987.3:c.*949T>C	XP_005255044.1:n.*949T>C
XM_006720759.2:c.*1000T>C	XP_006720822.1:n.*1000T>C
XM_006720760.2:c.*412T>C	XP_006720823.1:n.*412T>C
XM_011522187.2:c.*354T>C	XP_011520489.1:n.*354T>C
XM_011522188.3:c.*354T>C	XP_011520490.1:n.*354T>C
XM_011522189.2:c.*354T>C	XP_011520491.1:n.*354T>C
XM_011522191.3:c.*451T>C	XP_011520493.1:n.*451T>C
XM_011522192.2:c.*354T>C	XP_011520494.1:n.*354T>C
XM_017022712.2:c.*906T>C	XP_016878201.1:n.*906T>C
XM_017022713.2:c.*906T>C	XP_016878202.1:n.*906T>C
XM_017022715.2:c.*906T>C	XP_016878204.1:n.*906T>C
XM_017022716.2:c.*906T>C	XP_016878205.1:n.*906T>C
XM_017022717.1:c.*949T>C	XP_016878206.1:n.*949T>C
NM_003981.4:c.*906T>C MANE Select	NP_003972.2:n.*906T>C
NM_001267580.2:c.*949T>C	NP_001254509.2:n.*949T>C
NM_199413.3:c.*906T>C	NP_955445.2:n.*906T>C