Canonical Allele Identifier: CA717053273

Gene: PRC1 PRC1-AS1

Linked Data

• dbSNP Id: rs1237425950
• gnomAD v3: 15-90966748-G-GTTACAGGT
• gnomAD v4: 15-90966748-G-GTTACAGGT
• MyVariant Identifiers: chr15:g.91509978_91509979insTTACAGGT (hg19) ; chr15:g.90966748_90966749insTTACAGGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966749_90966756dup , CM000677.2:g.90966749_90966756dup	GRCh38
NC_000015.9:g.91509979_91509986dup , CM000677.1:g.91509979_91509986dup	GRCh37
NC_000015.8:g.89310983_89310990dup	NCBI36
NG_050647.1:g.32896_32903dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*375_*382dup (PRC1) MANE Select	ENSP00000377793.3:n.*375_*382dup
ENST00000643536.1:c.*4000_*4007dup	ENSP00000494429.1:n.*4000_*4007dup
ENST00000361188.9:c.*375_*382dup (PRC1)	ENSP00000354679.5:n.*375_*382dup
ENST00000394249.7:c.*375_*382dup (PRC1)	ENSP00000377793.3:n.*375_*382dup
ENST00000555455.5:c.642-103_642-96dup (PRC1)
ENST00000556972.6:c.125-103_125-96dup (PRC1)	ENSP00000456737.1:n.125-103_125-96dup
ENST00000560423.5:c.663_670dup (PRC1)
NM_001267580.1:c.*418_*425dup (PRC1)	NP_001254509.1:n.*418_*425dup
NM_003981.3:c.*375_*382dup (PRC1)	NP_003972.1:n.*375_*382dup
NM_199413.2:c.*375_*382dup (PRC1)	NP_955445.1:n.*375_*382dup
NR_051984.1:n.310+71_310+78dup (PRC1-AS1)
XM_005254987.1:c.*418_*425dup (PRC1)	XP_005255044.1:n.*418_*425dup
XM_006720759.1:c.*469_*476dup (PRC1)	XP_006720822.1:n.*469_*476dup
XM_006720760.1:c.1673-103_1673-96dup (PRC1)	XP_006720823.1:n.1673-103_1673-96dup
XM_011522187.1:c.1792-103_1792-96dup (PRC1)	XP_011520489.1:n.1792-103_1792-96dup
XM_011522188.1:c.1750-103_1750-96dup (PRC1)	XP_011520490.1:n.1750-103_1750-96dup
XM_011522189.1:c.1681-103_1681-96dup (PRC1)	XP_011520491.1:n.1681-103_1681-96dup
XM_011522190.1:c.1621-103_1621-96dup (PRC1)	XP_011520492.1:n.1621-103_1621-96dup
XM_011522191.1:c.*23-103_*23-96dup (PRC1)	XP_011520493.1:n.*23-103_*23-96dup
XM_011522192.1:c.1471-103_1471-96dup (PRC1)	XP_011520494.1:n.1471-103_1471-96dup
XM_005254987.3:c.*418_*425dup (PRC1)	XP_005255044.1:n.*418_*425dup
XM_006720759.2:c.*469_*476dup (PRC1)	XP_006720822.1:n.*469_*476dup
XM_006720760.2:c.1673-103_1673-96dup (PRC1)	XP_006720823.1:n.1673-103_1673-96dup
XM_011522187.2:c.1792-103_1792-96dup (PRC1)	XP_011520489.1:n.1792-103_1792-96dup
XM_011522188.3:c.1750-103_1750-96dup (PRC1)	XP_011520490.1:n.1750-103_1750-96dup
XM_011522189.2:c.1681-103_1681-96dup (PRC1)	XP_011520491.1:n.1681-103_1681-96dup
XM_011522190.3:c.1621-103_1621-96dup (PRC1)	XP_011520492.1:n.1621-103_1621-96dup
XM_011522191.3:c.*23-103_*23-96dup (PRC1)	XP_011520493.1:n.*23-103_*23-96dup
XM_011522192.2:c.1471-103_1471-96dup (PRC1)	XP_011520494.1:n.1471-103_1471-96dup
XM_017022712.2:c.*375_*382dup (PRC1)	XP_016878201.1:n.*375_*382dup
XM_017022713.2:c.*375_*382dup (PRC1)	XP_016878202.1:n.*375_*382dup
XM_017022714.2:c.1636-103_1636-96dup (PRC1)	XP_016878203.1:n.1636-103_1636-96dup
XM_017022715.2:c.*375_*382dup (PRC1)	XP_016878204.1:n.*375_*382dup
XM_017022716.2:c.*375_*382dup (PRC1)	XP_016878205.1:n.*375_*382dup
XM_017022717.1:c.*418_*425dup (PRC1)	XP_016878206.1:n.*418_*425dup
NM_003981.4:c.*375_*382dup (PRC1) MANE Select	NP_003972.2:n.*375_*382dup
NM_001267580.2:c.*418_*425dup (PRC1)	NP_001254509.2:n.*418_*425dup
NM_199413.3:c.*375_*382dup (PRC1)	NP_955445.2:n.*375_*382dup