Canonical Allele Identifier: CA274770678

Gene: PRC1

Linked Data

• dbSNP Id: rs757068375
• gnomAD v4: 15-90966235-CAAG-C
• MyVariant Identifiers: chr15:g.91509466_91509468del (hg19) ; chr15:g.90966236_90966238del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966240_90966242del , CM000677.2:g.90966240_90966242del	GRCh38
NC_000015.9:g.91509470_91509472del , CM000677.1:g.91509470_91509472del	GRCh37
NC_000015.8:g.89310474_89310476del	NCBI36
NG_050647.1:g.33414_33416del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*893_*895del MANE Select	ENSP00000377793.3:n.*893_*895del
ENST00000643536.1:c.*4518_*4520del	ENSP00000494429.1:n.*4518_*4520del
ENST00000361188.9:c.*893_*895del	ENSP00000354679.5:n.*893_*895del
ENST00000394249.7:c.*893_*895del	ENSP00000377793.3:n.*893_*895del
ENST00000556972.6:c.540_542del	ENSP00000456737.1:n.540_542del
NM_001267580.1:c.*936_*938del	NP_001254509.1:n.*936_*938del
NM_003981.3:c.*893_*895del	NP_003972.1:n.*893_*895del
NM_199413.2:c.*893_*895del	NP_955445.1:n.*893_*895del
XM_005254987.1:c.*936_*938del	XP_005255044.1:n.*936_*938del
XM_006720759.1:c.*987_*989del	XP_006720822.1:n.*987_*989del
XM_006720760.1:c.*399_*401del	XP_006720823.1:n.*399_*401del
XM_011522187.1:c.*341_*343del	XP_011520489.1:n.*341_*343del
XM_011522188.1:c.*341_*343del	XP_011520490.1:n.*341_*343del
XM_011522189.1:c.*341_*343del	XP_011520491.1:n.*341_*343del
XM_011522190.1:c.*341_*343del	XP_011520492.1:n.*341_*343del
XM_011522192.1:c.*341_*343del	XP_011520494.1:n.*341_*343del
XM_005254987.3:c.*936_*938del	XP_005255044.1:n.*936_*938del
XM_006720759.2:c.*987_*989del	XP_006720822.1:n.*987_*989del
XM_006720760.2:c.*399_*401del	XP_006720823.1:n.*399_*401del
XM_011522187.2:c.*341_*343del	XP_011520489.1:n.*341_*343del
XM_011522188.3:c.*341_*343del	XP_011520490.1:n.*341_*343del
XM_011522189.2:c.*341_*343del	XP_011520491.1:n.*341_*343del
XM_011522191.3:c.*438_*440del	XP_011520493.1:n.*438_*440del
XM_011522192.2:c.*341_*343del	XP_011520494.1:n.*341_*343del
XM_017022712.2:c.*893_*895del	XP_016878201.1:n.*893_*895del
XM_017022713.2:c.*893_*895del	XP_016878202.1:n.*893_*895del
XM_017022715.2:c.*893_*895del	XP_016878204.1:n.*893_*895del
XM_017022716.2:c.*893_*895del	XP_016878205.1:n.*893_*895del
XM_017022717.1:c.*936_*938del	XP_016878206.1:n.*936_*938del
NM_003981.4:c.*893_*895del MANE Select	NP_003972.2:n.*893_*895del
NM_001267580.2:c.*936_*938del	NP_001254509.2:n.*936_*938del
NM_199413.3:c.*893_*895del	NP_955445.2:n.*893_*895del