Canonical Allele Identifier: CA619861965

Gene: PRC1

Linked Data

• dbSNP Id: rs1255036821
• gnomAD v2: 15-91509595-G-GAACA
• gnomAD v3: 15-90966365-G-GAACA
• gnomAD v4: 15-90966365-G-GAACA
• MyVariant Identifiers: chr15:g.91509595_91509596insAACA (hg19) ; chr15:g.90966365_90966366insAACA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966370_90966373dup , CM000677.2:g.90966370_90966373dup	GRCh38
NC_000015.9:g.91509600_91509603dup , CM000677.1:g.91509600_91509603dup	GRCh37
NC_000015.8:g.89310604_89310607dup	NCBI36
NG_050647.1:g.33283_33286dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000394249.8:c.*762_*765dup MANE Select	ENSP00000377793.3:n.*762_*765dup
ENST00000643536.1:c.*4387_*4390dup	ENSP00000494429.1:n.*4387_*4390dup
ENST00000361188.9:c.*762_*765dup	ENSP00000354679.5:n.*762_*765dup
ENST00000394249.7:c.*762_*765dup	ENSP00000377793.3:n.*762_*765dup
ENST00000556972.6:c.409_412dup	ENSP00000456737.1:n.409_412dup
NM_001267580.1:c.*805_*808dup	NP_001254509.1:n.*805_*808dup
NM_003981.3:c.*762_*765dup	NP_003972.1:n.*762_*765dup
NM_199413.2:c.*762_*765dup	NP_955445.1:n.*762_*765dup
XM_005254987.1:c.*805_*808dup	XP_005255044.1:n.*805_*808dup
XM_006720759.1:c.*856_*859dup	XP_006720822.1:n.*856_*859dup
XM_006720760.1:c.*268_*271dup	XP_006720823.1:n.*268_*271dup
XM_011522187.1:c.*210_*213dup	XP_011520489.1:n.*210_*213dup
XM_011522188.1:c.*210_*213dup	XP_011520490.1:n.*210_*213dup
XM_011522189.1:c.*210_*213dup	XP_011520491.1:n.*210_*213dup
XM_011522190.1:c.*210_*213dup	XP_011520492.1:n.*210_*213dup
XM_011522192.1:c.*210_*213dup	XP_011520494.1:n.*210_*213dup
XM_005254987.3:c.*805_*808dup	XP_005255044.1:n.*805_*808dup
XM_006720759.2:c.*856_*859dup	XP_006720822.1:n.*856_*859dup
XM_006720760.2:c.*268_*271dup	XP_006720823.1:n.*268_*271dup
XM_011522187.2:c.*210_*213dup	XP_011520489.1:n.*210_*213dup
XM_011522188.3:c.*210_*213dup	XP_011520490.1:n.*210_*213dup
XM_011522189.2:c.*210_*213dup	XP_011520491.1:n.*210_*213dup
XM_011522191.3:c.*307_*310dup	XP_011520493.1:n.*307_*310dup
XM_011522192.2:c.*210_*213dup	XP_011520494.1:n.*210_*213dup
XM_017022712.2:c.*762_*765dup	XP_016878201.1:n.*762_*765dup
XM_017022713.2:c.*762_*765dup	XP_016878202.1:n.*762_*765dup
XM_017022715.2:c.*762_*765dup	XP_016878204.1:n.*762_*765dup
XM_017022716.2:c.*762_*765dup	XP_016878205.1:n.*762_*765dup
XM_017022717.1:c.*805_*808dup	XP_016878206.1:n.*805_*808dup
NM_003981.4:c.*762_*765dup MANE Select	NP_003972.2:n.*762_*765dup
NM_001267580.2:c.*805_*808dup	NP_001254509.2:n.*805_*808dup
NM_199413.3:c.*762_*765dup	NP_955445.2:n.*762_*765dup