Canonical Allele Identifier: CA393870674

Gene: PRC1 PRC1-AS1

Linked Data

• MyVariant Identifiers: chr15:g.91509875A>G (hg19) ; chr15:g.90966645A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966645A>G , CM000677.2:g.90966645A>G	GRCh38
NC_000015.9:g.91509875A>G , CM000677.1:g.91509875A>G	GRCh37
NC_000015.8:g.89310879A>G	NCBI36
NG_050647.1:g.33007T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*486T>C (PRC1) MANE Select	ENSP00000377793.3:n.*486T>C
ENST00000643536.1:c.*4111T>C	ENSP00000494429.1:n.*4111T>C
ENST00000361188.9:c.*486T>C (PRC1)	ENSP00000354679.5:n.*486T>C
ENST00000394249.7:c.*486T>C (PRC1)	ENSP00000377793.3:n.*486T>C
ENST00000555455.5:c.650T>C (PRC1)
ENST00000556972.6:c.133T>C (PRC1)	ENSP00000456737.1:p.Ser45Pro
NM_001267580.1:c.*529T>C (PRC1)	NP_001254509.1:n.*529T>C
NM_003981.3:c.*486T>C (PRC1)	NP_003972.1:n.*486T>C
NM_199413.2:c.*486T>C (PRC1)	NP_955445.1:n.*486T>C
NR_051984.1:n.277A>G (PRC1-AS1)
XM_005254987.1:c.*529T>C (PRC1)	XP_005255044.1:n.*529T>C
XM_006720759.1:c.*580T>C (PRC1)	XP_006720822.1:n.*580T>C
XM_006720760.1:c.1681T>C (PRC1)	XP_006720823.1:p.Ser561Pro
XM_011522187.1:c.1800T>C (PRC1)	XP_011520489.1:p.Leu600=
XM_011522188.1:c.1758T>C (PRC1)	XP_011520490.1:p.Leu586=
XM_011522189.1:c.1689T>C (PRC1)	XP_011520491.1:p.Leu563=
XM_011522190.1:c.1629T>C (PRC1)	XP_011520492.1:p.Leu543=
XM_011522191.1:c.*31T>C (PRC1)	XP_011520493.1:n.*31T>C
XM_011522192.1:c.1479T>C (PRC1)	XP_011520494.1:p.Leu493=
XM_005254987.3:c.*529T>C (PRC1)	XP_005255044.1:n.*529T>C
XM_006720759.2:c.*580T>C (PRC1)	XP_006720822.1:n.*580T>C
XM_006720760.2:c.1681T>C (PRC1)	XP_006720823.1:p.Ser561Pro
XM_011522187.2:c.1800T>C (PRC1)	XP_011520489.1:p.Leu600=
XM_011522188.3:c.1758T>C (PRC1)	XP_011520490.1:p.Leu586=
XM_011522189.2:c.1689T>C (PRC1)	XP_011520491.1:p.Leu563=
XM_011522190.3:c.1629T>C (PRC1)	XP_011520492.1:p.Leu543=
XM_011522191.3:c.*31T>C (PRC1)	XP_011520493.1:n.*31T>C
XM_011522192.2:c.1479T>C (PRC1)	XP_011520494.1:p.Leu493=
XM_017022712.2:c.*486T>C (PRC1)	XP_016878201.1:n.*486T>C
XM_017022713.2:c.*486T>C (PRC1)	XP_016878202.1:n.*486T>C
XM_017022714.2:c.1644T>C (PRC1)	XP_016878203.1:p.Leu548=
XM_017022715.2:c.*486T>C (PRC1)	XP_016878204.1:n.*486T>C
XM_017022716.2:c.*486T>C (PRC1)	XP_016878205.1:n.*486T>C
XM_017022717.1:c.*529T>C (PRC1)	XP_016878206.1:n.*529T>C
NM_003981.4:c.*486T>C (PRC1) MANE Select	NP_003972.2:n.*486T>C
NM_001267580.2:c.*529T>C (PRC1)	NP_001254509.2:n.*529T>C
NM_199413.3:c.*486T>C (PRC1)	NP_955445.2:n.*486T>C