Canonical Allele Identifier: CA492187237

Gene: PRC1 PRC1-AS1

Linked Data

• MyVariant Identifiers: chr15:g.91509635A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966405A>G , CM000677.2:g.90966405A>G	GRCh38
NC_000015.9:g.91509635A>G , CM000677.1:g.91509635A>G	GRCh37
NC_000015.8:g.89310639A>G	NCBI36
NG_050647.1:g.33247T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*726T>C (PRC1) MANE Select	ENSP00000377793.3:n.*726T>C
ENST00000643536.1:c.*4351T>C	ENSP00000494429.1:n.*4351T>C
ENST00000361188.9:c.*726T>C (PRC1)	ENSP00000354679.5:n.*726T>C
ENST00000394249.7:c.*726T>C (PRC1)	ENSP00000377793.3:n.*726T>C
ENST00000556972.6:c.373T>C (PRC1)	ENSP00000456737.1:n.373T>C
NM_001267580.1:c.*769T>C (PRC1)	NP_001254509.1:n.*769T>C
NM_003981.3:c.*726T>C (PRC1)	NP_003972.1:n.*726T>C
NM_199413.2:c.*726T>C (PRC1)	NP_955445.1:n.*726T>C
NR_051984.1:n.37A>G (PRC1-AS1)
XM_005254987.1:c.*769T>C (PRC1)	XP_005255044.1:n.*769T>C
XM_006720759.1:c.*820T>C (PRC1)	XP_006720822.1:n.*820T>C
XM_006720760.1:c.*232T>C (PRC1)	XP_006720823.1:n.*232T>C
XM_011522187.1:c.*174T>C (PRC1)	XP_011520489.1:n.*174T>C
XM_011522188.1:c.*174T>C (PRC1)	XP_011520490.1:n.*174T>C
XM_011522189.1:c.*174T>C (PRC1)	XP_011520491.1:n.*174T>C
XM_011522190.1:c.*174T>C (PRC1)	XP_011520492.1:n.*174T>C
XM_011522192.1:c.*174T>C (PRC1)	XP_011520494.1:n.*174T>C
XM_005254987.3:c.*769T>C (PRC1)	XP_005255044.1:n.*769T>C
XM_006720759.2:c.*820T>C (PRC1)	XP_006720822.1:n.*820T>C
XM_006720760.2:c.*232T>C (PRC1)	XP_006720823.1:n.*232T>C
XM_011522187.2:c.*174T>C (PRC1)	XP_011520489.1:n.*174T>C
XM_011522188.3:c.*174T>C (PRC1)	XP_011520490.1:n.*174T>C
XM_011522189.2:c.*174T>C (PRC1)	XP_011520491.1:n.*174T>C
XM_011522191.3:c.*271T>C (PRC1)	XP_011520493.1:n.*271T>C
XM_011522192.2:c.*174T>C (PRC1)	XP_011520494.1:n.*174T>C
XM_017022712.2:c.*726T>C (PRC1)	XP_016878201.1:n.*726T>C
XM_017022713.2:c.*726T>C (PRC1)	XP_016878202.1:n.*726T>C
XM_017022715.2:c.*726T>C (PRC1)	XP_016878204.1:n.*726T>C
XM_017022716.2:c.*726T>C (PRC1)	XP_016878205.1:n.*726T>C
XM_017022717.1:c.*769T>C (PRC1)	XP_016878206.1:n.*769T>C
NM_003981.4:c.*726T>C (PRC1) MANE Select	NP_003972.2:n.*726T>C
NM_001267580.2:c.*769T>C (PRC1)	NP_001254509.2:n.*769T>C
NM_199413.3:c.*726T>C (PRC1)	NP_955445.2:n.*726T>C