Canonical Allele Identifier: CA2739484729

Gene: PRC1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966318A>T , CM000677.2:g.90966318A>T	GRCh38
NC_000015.9:g.91509548A>T , CM000677.1:g.91509548A>T	GRCh37
NC_000015.8:g.89310552A>T	NCBI36
NG_050647.1:g.33334T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*813T>A MANE Select	ENSP00000377793.3:n.*813T>A
ENST00000643536.1:c.*4438T>A	ENSP00000494429.1:n.*4438T>A
ENST00000361188.9:c.*813T>A	ENSP00000354679.5:n.*813T>A
ENST00000394249.7:c.*813T>A	ENSP00000377793.3:n.*813T>A
ENST00000556972.6:c.460T>A	ENSP00000456737.1:n.460T>A
NM_001267580.1:c.*856T>A	NP_001254509.1:n.*856T>A
NM_003981.3:c.*813T>A	NP_003972.1:n.*813T>A
NM_199413.2:c.*813T>A	NP_955445.1:n.*813T>A
XM_005254987.1:c.*856T>A	XP_005255044.1:n.*856T>A
XM_006720759.1:c.*907T>A	XP_006720822.1:n.*907T>A
XM_006720760.1:c.*319T>A	XP_006720823.1:n.*319T>A
XM_011522187.1:c.*261T>A	XP_011520489.1:n.*261T>A
XM_011522188.1:c.*261T>A	XP_011520490.1:n.*261T>A
XM_011522189.1:c.*261T>A	XP_011520491.1:n.*261T>A
XM_011522190.1:c.*261T>A	XP_011520492.1:n.*261T>A
XM_011522192.1:c.*261T>A	XP_011520494.1:n.*261T>A
XM_005254987.3:c.*856T>A	XP_005255044.1:n.*856T>A
XM_006720759.2:c.*907T>A	XP_006720822.1:n.*907T>A
XM_006720760.2:c.*319T>A	XP_006720823.1:n.*319T>A
XM_011522187.2:c.*261T>A	XP_011520489.1:n.*261T>A
XM_011522188.3:c.*261T>A	XP_011520490.1:n.*261T>A
XM_011522189.2:c.*261T>A	XP_011520491.1:n.*261T>A
XM_011522191.3:c.*358T>A	XP_011520493.1:n.*358T>A
XM_011522192.2:c.*261T>A	XP_011520494.1:n.*261T>A
XM_017022712.2:c.*813T>A	XP_016878201.1:n.*813T>A
XM_017022713.2:c.*813T>A	XP_016878202.1:n.*813T>A
XM_017022715.2:c.*813T>A	XP_016878204.1:n.*813T>A
XM_017022716.2:c.*813T>A	XP_016878205.1:n.*813T>A
XM_017022717.1:c.*856T>A	XP_016878206.1:n.*856T>A
NM_003981.4:c.*813T>A MANE Select	NP_003972.2:n.*813T>A
NM_001267580.2:c.*856T>A	NP_001254509.2:n.*856T>A
NM_199413.3:c.*813T>A	NP_955445.2:n.*813T>A