Canonical Allele Identifier: CA2739484716

Gene: PRC1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966312A>C , CM000677.2:g.90966312A>C	GRCh38
NC_000015.9:g.91509542A>C , CM000677.1:g.91509542A>C	GRCh37
NC_000015.8:g.89310546A>C	NCBI36
NG_050647.1:g.33340T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*819T>G MANE Select	ENSP00000377793.3:n.*819T>G
ENST00000643536.1:c.*4444T>G	ENSP00000494429.1:n.*4444T>G
ENST00000361188.9:c.*819T>G	ENSP00000354679.5:n.*819T>G
ENST00000394249.7:c.*819T>G	ENSP00000377793.3:n.*819T>G
ENST00000556972.6:c.466T>G	ENSP00000456737.1:n.466T>G
NM_001267580.1:c.*862T>G	NP_001254509.1:n.*862T>G
NM_003981.3:c.*819T>G	NP_003972.1:n.*819T>G
NM_199413.2:c.*819T>G	NP_955445.1:n.*819T>G
XM_005254987.1:c.*862T>G	XP_005255044.1:n.*862T>G
XM_006720759.1:c.*913T>G	XP_006720822.1:n.*913T>G
XM_006720760.1:c.*325T>G	XP_006720823.1:n.*325T>G
XM_011522187.1:c.*267T>G	XP_011520489.1:n.*267T>G
XM_011522188.1:c.*267T>G	XP_011520490.1:n.*267T>G
XM_011522189.1:c.*267T>G	XP_011520491.1:n.*267T>G
XM_011522190.1:c.*267T>G	XP_011520492.1:n.*267T>G
XM_011522192.1:c.*267T>G	XP_011520494.1:n.*267T>G
XM_005254987.3:c.*862T>G	XP_005255044.1:n.*862T>G
XM_006720759.2:c.*913T>G	XP_006720822.1:n.*913T>G
XM_006720760.2:c.*325T>G	XP_006720823.1:n.*325T>G
XM_011522187.2:c.*267T>G	XP_011520489.1:n.*267T>G
XM_011522188.3:c.*267T>G	XP_011520490.1:n.*267T>G
XM_011522189.2:c.*267T>G	XP_011520491.1:n.*267T>G
XM_011522191.3:c.*364T>G	XP_011520493.1:n.*364T>G
XM_011522192.2:c.*267T>G	XP_011520494.1:n.*267T>G
XM_017022712.2:c.*819T>G	XP_016878201.1:n.*819T>G
XM_017022713.2:c.*819T>G	XP_016878202.1:n.*819T>G
XM_017022715.2:c.*819T>G	XP_016878204.1:n.*819T>G
XM_017022716.2:c.*819T>G	XP_016878205.1:n.*819T>G
XM_017022717.1:c.*862T>G	XP_016878206.1:n.*862T>G
NM_003981.4:c.*819T>G MANE Select	NP_003972.2:n.*819T>G
NM_001267580.2:c.*862T>G	NP_001254509.2:n.*862T>G
NM_199413.3:c.*819T>G	NP_955445.2:n.*819T>G