Canonical Allele Identifier: CA2195381073

Gene: PRC1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966254_90966255delinsGA , CM000677.2:g.90966254_90966255delinsGA	GRCh38
NC_000015.9:g.91509484_91509485delinsGA , CM000677.1:g.91509484_91509485delinsGA	GRCh37
NC_000015.8:g.89310488_89310489delinsGA	NCBI36
NG_050647.1:g.33397_33398delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*876_*877delinsTC MANE Select	ENSP00000377793.3:n.*876_*877delinsTC
ENST00000643536.1:c.*4501_*4502delinsTC	ENSP00000494429.1:n.*4501_*4502delinsTC
ENST00000361188.9:c.*876_*877delinsTC	ENSP00000354679.5:n.*876_*877delinsTC
ENST00000394249.7:c.*876_*877delinsTC	ENSP00000377793.3:n.*876_*877delinsTC
ENST00000556972.6:c.523_524delinsTC	ENSP00000456737.1:n.523_524delinsTC
NM_001267580.1:c.*919_*920delinsTC	NP_001254509.1:n.*919_*920delinsTC
NM_003981.3:c.*876_*877delinsTC	NP_003972.1:n.*876_*877delinsTC
NM_199413.2:c.*876_*877delinsTC	NP_955445.1:n.*876_*877delinsTC
XM_005254987.1:c.*919_*920delinsTC	XP_005255044.1:n.*919_*920delinsTC
XM_006720759.1:c.*970_*971delinsTC	XP_006720822.1:n.*970_*971delinsTC
XM_006720760.1:c.*382_*383delinsTC	XP_006720823.1:n.*382_*383delinsTC
XM_011522187.1:c.*324_*325delinsTC	XP_011520489.1:n.*324_*325delinsTC
XM_011522188.1:c.*324_*325delinsTC	XP_011520490.1:n.*324_*325delinsTC
XM_011522189.1:c.*324_*325delinsTC	XP_011520491.1:n.*324_*325delinsTC
XM_011522190.1:c.*324_*325delinsTC	XP_011520492.1:n.*324_*325delinsTC
XM_011522192.1:c.*324_*325delinsTC	XP_011520494.1:n.*324_*325delinsTC
XM_005254987.3:c.*919_*920delinsTC	XP_005255044.1:n.*919_*920delinsTC
XM_006720759.2:c.*970_*971delinsTC	XP_006720822.1:n.*970_*971delinsTC
XM_006720760.2:c.*382_*383delinsTC	XP_006720823.1:n.*382_*383delinsTC
XM_011522187.2:c.*324_*325delinsTC	XP_011520489.1:n.*324_*325delinsTC
XM_011522188.3:c.*324_*325delinsTC	XP_011520490.1:n.*324_*325delinsTC
XM_011522189.2:c.*324_*325delinsTC	XP_011520491.1:n.*324_*325delinsTC
XM_011522191.3:c.*421_*422delinsTC	XP_011520493.1:n.*421_*422delinsTC
XM_011522192.2:c.*324_*325delinsTC	XP_011520494.1:n.*324_*325delinsTC
XM_017022712.2:c.*876_*877delinsTC	XP_016878201.1:n.*876_*877delinsTC
XM_017022713.2:c.*876_*877delinsTC	XP_016878202.1:n.*876_*877delinsTC
XM_017022715.2:c.*876_*877delinsTC	XP_016878204.1:n.*876_*877delinsTC
XM_017022716.2:c.*876_*877delinsTC	XP_016878205.1:n.*876_*877delinsTC
XM_017022717.1:c.*919_*920delinsTC	XP_016878206.1:n.*919_*920delinsTC
NM_003981.4:c.*876_*877delinsTC MANE Select	NP_003972.2:n.*876_*877delinsTC
NM_001267580.2:c.*919_*920delinsTC	NP_001254509.2:n.*919_*920delinsTC
NM_199413.3:c.*876_*877delinsTC	NP_955445.2:n.*876_*877delinsTC