Canonical Allele Identifier: CA2195380962

Gene: PRC1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966187_90966188delinsCA , CM000677.2:g.90966187_90966188delinsCA	GRCh38
NC_000015.9:g.91509417_91509418delinsCA , CM000677.1:g.91509417_91509418delinsCA	GRCh37
NC_000015.8:g.89310421_89310422delinsCA	NCBI36
NG_050647.1:g.33464_33465delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*943_*944delinsTG MANE Select	ENSP00000377793.3:n.*943_*944delinsTG
ENST00000361188.9:c.*943_*944delinsTG	ENSP00000354679.5:n.*943_*944delinsTG
ENST00000394249.7:c.*943_*944delinsTG	ENSP00000377793.3:n.*943_*944delinsTG
ENST00000556972.6:c.590_591delinsTG	ENSP00000456737.1:n.590_591delinsTG
NM_001267580.1:c.*986_*987delinsTG	NP_001254509.1:n.*986_*987delinsTG
NM_003981.3:c.*943_*944delinsTG	NP_003972.1:n.*943_*944delinsTG
NM_199413.2:c.*943_*944delinsTG	NP_955445.1:n.*943_*944delinsTG
XM_005254987.1:c.*986_*987delinsTG	XP_005255044.1:n.*986_*987delinsTG
XM_006720759.1:c.*1037_*1038delinsTG	XP_006720822.1:n.*1037_*1038delinsTG
XM_006720760.1:c.*449_*450delinsTG	XP_006720823.1:n.*449_*450delinsTG
XM_011522187.1:c.*391_*392delinsTG	XP_011520489.1:n.*391_*392delinsTG
XM_011522188.1:c.*391_*392delinsTG	XP_011520490.1:n.*391_*392delinsTG
XM_011522189.1:c.*391_*392delinsTG	XP_011520491.1:n.*391_*392delinsTG
XM_011522190.1:c.*391_*392delinsTG	XP_011520492.1:n.*391_*392delinsTG
XM_011522192.1:c.*391_*392delinsTG	XP_011520494.1:n.*391_*392delinsTG
XM_005254987.3:c.*986_*987delinsTG	XP_005255044.1:n.*986_*987delinsTG
XM_006720759.2:c.*1037_*1038delinsTG	XP_006720822.1:n.*1037_*1038delinsTG
XM_006720760.2:c.*449_*450delinsTG	XP_006720823.1:n.*449_*450delinsTG
XM_011522187.2:c.*391_*392delinsTG	XP_011520489.1:n.*391_*392delinsTG
XM_011522188.3:c.*391_*392delinsTG	XP_011520490.1:n.*391_*392delinsTG
XM_011522189.2:c.*391_*392delinsTG	XP_011520491.1:n.*391_*392delinsTG
XM_011522191.3:c.*488_*489delinsTG	XP_011520493.1:n.*488_*489delinsTG
XM_011522192.2:c.*391_*392delinsTG	XP_011520494.1:n.*391_*392delinsTG
XM_017022712.2:c.*943_*944delinsTG	XP_016878201.1:n.*943_*944delinsTG
XM_017022713.2:c.*943_*944delinsTG	XP_016878202.1:n.*943_*944delinsTG
XM_017022715.2:c.*943_*944delinsTG	XP_016878204.1:n.*943_*944delinsTG
XM_017022716.2:c.*943_*944delinsTG	XP_016878205.1:n.*943_*944delinsTG
XM_017022717.1:c.*986_*987delinsTG	XP_016878206.1:n.*986_*987delinsTG
NM_003981.4:c.*943_*944delinsTG MANE Select	NP_003972.2:n.*943_*944delinsTG
NM_001267580.2:c.*986_*987delinsTG	NP_001254509.2:n.*986_*987delinsTG
NM_199413.3:c.*943_*944delinsTG	NP_955445.2:n.*943_*944delinsTG