Canonical Allele Identifier: CA274789146

Gene: PRC1 PRC1-AS1

Linked Data

• dbSNP Id: rs1867226
• gnomAD v2: 15-91523713-C-G
• gnomAD v3: 15-90980483-C-G
• gnomAD v4: 15-90980483-C-G
• MyVariant Identifiers: chr15:g.91523713C>G (hg19) ; chr15:g.90980483C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90980483C>G , CM000677.2:g.90980483C>G	GRCh38
NC_000015.9:g.91523713C>G , CM000677.1:g.91523713C>G	GRCh37
NC_000015.8:g.89324717C>G	NCBI36
NG_050647.1:g.19169G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394249.8:c.823-94G>C (PRC1) MANE Select	ENSP00000377793.3:n.823-94G>C
ENST00000643536.1:c.*786-94G>C	ENSP00000494429.1:n.*786-94G>C
ENST00000647331.1:c.*1251-94G>C	ENSP00000493953.1:n.*1251-94G>C
ENST00000361188.9:c.823-94G>C (PRC1)	ENSP00000354679.5:n.823-94G>C
ENST00000394249.7:c.823-94G>C (PRC1)	ENSP00000377793.3:n.823-94G>C
ENST00000442656.6:c.700-94G>C (PRC1)	ENSP00000409549.2:n.700-94G>C
ENST00000556982.1:n.349-94G>C (PRC1)
ENST00000560914.1:n.41G>C (PRC1)
NM_001267580.1:c.700-94G>C (PRC1)	NP_001254509.1:n.700-94G>C
NM_003981.3:c.823-94G>C (PRC1)	NP_003972.1:n.823-94G>C
NM_199413.2:c.823-94G>C (PRC1)	NP_955445.1:n.823-94G>C
NR_051984.1:n.311-1472C>G (PRC1-AS1)
XM_005254987.1:c.823-94G>C (PRC1)	XP_005255044.1:n.823-94G>C
XM_006720759.1:c.823-94G>C (PRC1)	XP_006720822.1:n.823-94G>C
XM_006720760.1:c.823-94G>C (PRC1)	XP_006720823.1:n.823-94G>C
XM_011522187.1:c.823-94G>C (PRC1)	XP_011520489.1:n.823-94G>C
XM_011522188.1:c.823-94G>C (PRC1)	XP_011520490.1:n.823-94G>C
XM_011522189.1:c.823-94G>C (PRC1)	XP_011520491.1:n.823-94G>C
XM_011522190.1:c.652-94G>C (PRC1)	XP_011520492.1:n.652-94G>C
XM_011522191.1:c.823-94G>C (PRC1)	XP_011520493.1:n.823-94G>C
XM_011522192.1:c.502-94G>C (PRC1)	XP_011520494.1:n.502-94G>C
XM_005254987.3:c.823-94G>C (PRC1)	XP_005255044.1:n.823-94G>C
XM_006720759.2:c.823-94G>C (PRC1)	XP_006720822.1:n.823-94G>C
XM_006720760.2:c.823-94G>C (PRC1)	XP_006720823.1:n.823-94G>C
XM_011522187.2:c.823-94G>C (PRC1)	XP_011520489.1:n.823-94G>C
XM_011522188.3:c.823-94G>C (PRC1)	XP_011520490.1:n.823-94G>C
XM_011522189.2:c.823-94G>C (PRC1)	XP_011520491.1:n.823-94G>C
XM_011522190.3:c.652-94G>C (PRC1)	XP_011520492.1:n.652-94G>C
XM_011522191.3:c.823-94G>C (PRC1)	XP_011520493.1:n.823-94G>C
XM_011522192.2:c.502-94G>C (PRC1)	XP_011520494.1:n.502-94G>C
XM_017022712.2:c.823-94G>C (PRC1)	XP_016878201.1:n.823-94G>C
XM_017022713.2:c.823-94G>C (PRC1)	XP_016878202.1:n.823-94G>C
XM_017022714.2:c.667-94G>C (PRC1)	XP_016878203.1:n.667-94G>C
XM_017022715.2:c.667-94G>C (PRC1)	XP_016878204.1:n.667-94G>C
XM_017022716.2:c.652-94G>C (PRC1)	XP_016878205.1:n.652-94G>C
XM_017022717.1:c.667-94G>C (PRC1)	XP_016878206.1:n.667-94G>C
NM_003981.4:c.823-94G>C (PRC1) MANE Select	NP_003972.2:n.823-94G>C
NM_001267580.2:c.700-94G>C (PRC1)	NP_001254509.2:n.700-94G>C
NM_199413.3:c.823-94G>C (PRC1)	NP_955445.2:n.823-94G>C