Canonical Allele Identifier: CA8845203
Gene: PYCR1 HGNC NCBI

Linked Data

dbSNP Id: rs747011017

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81932972del , CM000679.2:g.81932972del GRCh38
NC_000017.10:g.79890848del , CM000679.1:g.79890848del GRCh37
NC_000017.9:g.77484139del NCBI36
NG_023032.1:g.9122del

Transcript Alleles

HGVS Amino-acid Change
ENST00000329875.13:c.*243del MANE Select ENSP00000328858.8:n.*243del
ENST00000329875.12:c.*243del ENSP00000328858.8:n.*243del
ENST00000337943.9:c.868-8del ENSP00000336579.5:n.868-8del
ENST00000402252.6:c.*243del ENSP00000384949.2:n.*243del
ENST00000403172.8:c.*243del ENSP00000385483.4:n.*243del
ENST00000577756.5:c.*385del ENSP00000463352.1:n.*385del
ENST00000584848.5:c.907del ENSP00000463342.1:n.907del
ENST00000619204.4:c.*243del ENSP00000479793.1:n.*243del
ENST00000629768.2:c.*385del ENSP00000485679.1:n.*385del
NM_001282279.1:c.*243del NP_001269208.1:n.*243del
NM_001282280.1:c.*243del NP_001269209.1:n.*243del
NM_001282281.1:c.*243del NP_001269210.1:n.*243del
NM_006907.3:c.*243del NP_008838.2:n.*243del
NM_153824.2:c.868-8del NP_722546.1:n.868-8del
XM_005256381.1:c.*243del XP_005256438.1:n.*243del
XM_011523583.1:c.*243del XP_011521885.1:n.*243del
XM_011523584.1:c.*243del XP_011521886.1:n.*243del
XM_011523585.1:c.*385del XP_011521887.1:n.*385del
NM_001330523.1:c.*385del NP_001317452.1:n.*385del
XM_005256381.2:c.*243del XP_005256438.1:n.*243del
XM_011523583.2:c.*243del XP_011521885.1:n.*243del
XM_011523584.3:c.*243del XP_011521886.1:n.*243del
XM_011523585.2:c.*385del XP_011521887.1:n.*385del
XM_024450849.1:c.*243del XP_024306617.1:n.*243del
NM_001282279.2:c.*243del NP_001269208.1:n.*243del
NM_001282281.2:c.*243del NP_001269210.1:n.*243del
NM_006907.4:c.*243del MANE Select NP_008838.2:n.*243del
NM_153824.3:c.868-8del NP_722546.1:n.868-8del
NM_001282280.2:c.*243del NP_001269209.1:n.*243del
NM_001330523.2:c.*385del NP_001317452.1:n.*385del